Devices and methods for selective surgical removal of tissue

ABSTRACT

Methods and apparatus are provided for selective surgical removal of tissue. In one variation, tissue may be ablated, resected, removed, or otherwise remodeled by standard small endoscopic tools delivered into the epidural space through an epidural needle. The sharp tip of the needle in the epidural space, can be converted to a blunt tipped instrument for further safe advancement. The current invention includes specific tools that enable safe tissue modification in the epidural space, including a barrier that separates the area where tissue modification will take place from adjacent vulnerable neural and vascular structures. A nerve stimulator may be provided to reduce a risk of inadvertent neural abrasion.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Application No.60/619,306, filed 15 Oct. 2004 and U.S. Application No. 60/622,865,filed 28 Oct. 2004, each of which is incorporated by reference herein inits entirety.

FIELD OF THE INVENTION

The present invention relates to methods and apparatus for selectivesurgical removal of tissue, such as for the treatment of spinal neuraland neurovascular impingement, through selective resection, ablation,and remodeling of tissue in the lateral recess, neural foramina andcentral spinal canal, more particularly, for safely performing lateralrecess and neuroforaminal enlargement of the spine.

BACKGROUND OF THE INVENTION

Pathological compression of spinal neural and neurovascular structuresis an age-related process, increased in prevalence and severity inelderly populations, with potential congenital anatomic components, thatresult in back, radicular extremity pain and both neurological (e.g.,sensory) and mechanical (e.g., motor) dysfunction. Prevalence is alsoinfluenced by congenital spinal anatomy. Disease progression leads toincreased neural irritation, impingement, and ischemia, and isfrequently accompanied by progressively increased pain, often inconjunction with reflex, sensory and motor neurological deficits.

In the United States, Spinal Stenosis occurs with an incidence ofbetween 4 percent and 6 percent of adults 50 years of age or older, andis the most frequent reason cited for back surgery in patients 60 yearsof age and older.

Spinal Stenosis often includes neural or neurovascular impingement,which may occur in the central spinal canal, the lateral recesses of thespinal canal, or in the spinal neural foramina. The most common causesof neural compression within the spine are spinal disc disease(collapse, bulging, herniation); ligamentum flavum buckling, thickeningand/or hypertrophy; zygapophysial (facet) joint hypertrophy; osteophyteformation; and spondylolisthesis.

Disease progression increases neural irritation, impingement, andischemia, and is frequently accompanied by progressively increased pain,often in conjunction with reflex, sensory and motor neurologicaldeficits.

Current surgical treatments for Spinal Stenosis include laminectomy(usually partial, but sometimes complete) and/or facetectomy (usuallypartial, but sometimes complete), with or without fusion. While standardsurgical procedures lead to improvements in symptoms for 6 months ormore in approximately 60% of cases, there is an unacceptable incidenceof long-term complications and morbidity.

Several companies offer tools that facilitate surgical access to theareas of the spine where neural impingement is likely to occur, in orderto allow the surgeon to decompress the impinged neural structuresthrough the removal of vertebral lamina, ligamentum flavum, facetcomplex, bone spurs, and/or intervertebral disc material. These surgicalresections are frequently (i.e., occurs in 15% to 20% of cases)accompanied by fusion (arthrodesis). Spinal arthrodesis is performed tofuse adjacent vertebrae and prevent movement of these structures inrelation to each other. The fusion is commonly a treatment for pain ofpresumed disc or facet joint origin, for “unstable spines”, and forspines that have been rendered “unstable” by the surgical decompressionprocedures, as described above. The definition of “spinal instability”remains controversial in current literature.

Spinal arthrodesis may be achieved through various surgical techniques.Biocompatible metallic hardware and/or autograft or allograft bone iscommonly secured anteriorly and/or posteriorly in the vertebral columnin order to achieve surgical fusion. These materials are secured alongand between the vertebral bodies (to restore vertebral height andreplace disk material) and/or within the posterior elements, typicallywith pedicle screw fixation. Autograft bone is often harvested from thepatient's iliac crest. Cadaveric allograft is frequently cut in discshaped sections of long bones for replacement of the intervertebraldiscs in the fusion procedure.

Critics have frequently stated that, while discectomy and fusionprocedures frequently improve symptoms of neural impingement in theshort term, both are highly destructive procedures that diminish spinalfunction, drastically disrupt normal anatomy, and increase long-termmorbidity above levels seen in untreated patients.

The high morbidity associated with discectomy may be due to severalfactors. First, discectomy reduces disc height, causing increasedpressure on facet joints. This stress leads to facet arthritis and facetjoint hypertrophy, which then causes further neural compression. Thesurgically-imposed reduction in disc height also may led toneuroforaminal stenosis, as the vertebral pedicles, which form thesuperior and inferior borders of the neural foramina, become closer toone another. The loss of disc height also creates ligament laxity, whichmay lead to spondylolisthesis, spinal instability or osteophyte or “bonespur” formation, as it has been hypothesized that ligaments may calcifyin their attempt to become more “bone-like”. In addition, discectomyfrequently leads to an incised and further compromised disc annulus.This frequently leads to recurrent herniation of nuclear materialthrough the expanded annular opening. It may also cause further bucklingof the ligamentum flavum. The high morbidity associated with fusion isrelated to several factors. First, extensive hardware implantation maylead to complications due to breakage, loosening, nerve injury,infection, rejection, or scar tissue formation. In addition, autograftbone donor sites (typically the patient's iliac crest) are a frequentsource of complaints, such as infection, deformity, and protracted pain.Perhaps the most important reason for the long-term morbidity caused byspinal fusion is the loss of mobility in the fused segment of the spine.Not only do immobile vertebral segments lead to functional limitations,but they also cause increased stress on adjacent vertebral structures,thereby frequently accelerating the degeneration of other discs, joints,bone and other soft tissue structures within the spine.

Recently, less invasive, percutaneous approaches to spinal discectomyand fusion have been tried with some success. While these less invasivetechniques offer advantages, such as a quicker recovery and less tissuedestruction during the procedure, the new procedures do not diminish thefact that even less invasive spinal discectomy or fusion techniques areinherently destructive procedures that accelerate the onset of acquiredspinal stenosis and result in severe long-term consequences.

Additional less invasive treatments of neural impingement within thespine include percutaneous removal of nuclear disc material andprocedures that decrease the size and volume of the disc through thecreation of thermal disc injury. While these percutaneous procedures mayproduce less tissue injury, their efficacy remains unproven.

Even more recently, attempts have been made to replace pathologicaldiscs with prosthetic materials. While prosthetic disc replacement is arestorative procedure, it is a highly invasive and complex surgery. Anysynthetic lumbar disc will be required to withstand tremendousmechanical stresses and will require several years of development beforeit will achieve the longevity desired. Further, synthetic discs may notbe an appropriate therapeutic approach to a severely degenerative spine,where profound facet arthropathy and other changes are likely toincrease the complexity of disc replacement. Like most prostheticjoints, it is likely that synthetic discs will have a limited lifespanand that there will be continued need for minimally invasive techniquesthat delay the need for disc replacement. Even if prosthetic discsbecome a viable solution, a simpler, less invasive approach torestoration of functional spinal anatomy would play an important role inthe treatment of neural impingent in the spine. The artificial discs inU.S. clinical trials, as with any first generation prosthesis, are boundto fail in many cases, and will be very difficult to revise forpatients. The prostheses will, therefore, be best avoided, in manycases. Lumbar prosthetic discs are available in several countriesworldwide.

In view of the aforementioned limitations of prior art techniques fortreating neural and neurovascular impingement in the spine, it would bedesirable to provide methods and apparatus for selective surgicalremoval of tissue that reduce or overcome these limitations.

SUMMARY OF THE INVENTION

In view of the foregoing, the present invention provides apparatus andmethods for selective removal of tissue, e.g., soft tissue and bone,preferably in a minimally invasive fashion. An embodiment of the presentinvention provides apparatus and methods for safe and selective deliveryof surgical tools into to the epidural space; and for apparatus methodsthat enable safe and selective surgical removal, ablation, andremodeling of soft tissue and bone, preferably in a minimally invasivefashion, with the apparatus delivered into the epidural space. In animportant preferred variation of the methods and apparatusare used totreat neural and neurovascular impingement in the spine, through a novelapproach to safe and selective enlargement of the pathologically narrowspinal neural foramen, the impinged lateral recess, and central canal.

In a preferred embodiment, the methods and apparatus include theplacement of a working backstop or barrier into the epidural space orneural foramina, to a location between the tool positioned for tissuealteration, and adjacent vulnerable neural or vascular structures, tohelp prevent neural or vascular injury during surgery. In a furtherpreferred embodiment, the methods and apparatus utilize neuralstimulation techniques, to enable neural localization, as a means ofimproving the safety of the procedure.

In one variation of the present invention, an epidural needle may beconverted to a working tool in order to resect or remodel spinal tissue,which is enabled by the use of herein described methods and apparatus:

After placement of an epidural needle into the epidural space, a specialepidural catheter is threaded through the needle into the epiduralspace. This catheter apparatus contains a needle tip cover in its distalend, which, after it is converted to an open position in the epiduralspace, is pulled back over the needle tip, by pulling on the proximalportion of the catheter. The catheter based cover blunts and therebyprotects the vulnerable structures of the spine, such as the dura, fromthe sharp epidural needle tip. With the epidural needle tip covered, theneedle may be more safely advanced into the epidural space, in adirection somewhat parallel to the dura, towards the contralateral oripsilateral lateral recess and neural foramen. The needle may beadvanced blindly; with image guidance; or with endoscopic guidance.

The epidural catheter, with the cap or cover for the epidural needle,may or may not contain a rigid or flexible fiberoptic cable. With afiberoptic element and a clear tip to the catheter, the epidural needlemay be converted to an epidural endoscope or “needlescope”.

One preferred embodiment of the epidural needle apparatus contains twoadjacent lumens (“double barreled”), with a working channel adjacent tothe epidural needle. The working channel may be fixed and permanent, orremovable, as in with a rail and track connection. A removable workingchannel, in one embodiment, may be inserted or removed while the tip ofthe epidural needle remains in the epidural space. The distal beveledopening of the working channel, in a preferred variation, is locatedproximal to and on the same side of the needle as the epidural needletip beveled opening faces, facilitating visualization of the workingchannel tools when a fiberoptic element has been placed in through theepidural needle lumen.

The epidural needle or the working channel of the epidural needle may bea vehicle for insertion of a working backstop or barrier, anotherapparatus that facilitates safe tissue resection and remodeling in theepidural space. The barrier is a thin flat device that may be deliveredinto or adjacent to the epidural space or neural foramina, through theneedle or working channel, or through an endoscope or open incision.Such a backstop may consist of a flexible, curved, thin and flat pieceof material. This barrier will serve to protect neural and neurovascularstructures from being damaged during tissue manipulation and resection,because it will be placed between the tissue to be ablated, resected,irritated, manipulated or remodeled, and the vulnerable neural andvascular structures or dura. The tools for tissue resection and ablationwill be used on the side of the barrier opposite from the vulnerableneural and vascular structures, which will be safely protected frominadvertent injury.

In one variation of the present invention, a tissue abrasion device isplaced, either percutaneously or through an open surgical approach,through the neural foramina of the spine, around the anterior border ofthe facet joint, and anterior to the ligamentum flavum. The abrasiondevice alternatively or additionally may be placed through the neuralforamen anterior to the facet joint, but through or posterior to theligamentum flavum. After spinal neuroforaminal placement, the device isused to remove tissues that impinge on the neurovascular structureswithin the lateral recess and neural foramen, anterior to the facetjoint.

The abrasion device may, for example, include a thin belt or ribbon,with an abrasive, shaving, and/or cutting surface, which is placedthrough the neural foramina and is held firmly against the tissue to beremoved. The belt optionally may be placed, at least partially, within aprotective sheath or covering, with the treatment area exposed to theabrasive surface of the device somewhat limited to the area where tissueabrasion and removal is desired. The abrasive element may be provided inone or more of a variety of potentially interchangeable shapes, rangingfrom flat to curved; narrow to wide; or solid to perforated. Theabrasive surface may also have various enabling designs, or surfacepatterns, or coarseness of abrasive material. The apparatus is placedwith both free ends of the abrasive element, as well as the ends of theoptional protective sleeve or covering, external to the patient formanipulation by a medical practitioner.

When the optional protective sleeve or sheath is provided, both ends ofthe sleeve may be held under tension, external to the patient, such thatthe abrasive belt or ribbon may be pulled back and forth through thesleeve without causing significant friction against and/or trauma toadjacent tissues. Initially, both ends of the abrasive ribbon are pulledsimultaneously, pulling the device in a posterior and/or lateraldirection, thereby bringing impinging spinal tissue in contact with theabrasive and/or cutting surface of the ribbon. When one end of theribbon is pulled with more force than the other, the ribbon moves in thedirection of the stronger pull, while the lesser pull on the oppositeend maintains force and creates friction with movement between theabrasive surface and the tissue to be resected.

In an open surgical variation, the ribbon or belt and/or the protectivecovering or sleeve may be placed through the surgical incision. In apercutaneous variation, the device may be inserted through a needle orover a wire. As with the percutaneous approaches, placement may be aidedby the use of image guidance and/or the use of an epidural endoscope.

Once the surgical apparatus has been placed, the medical practitionermay enlarge the lateral recess and neural foramina via cutting, shaving,filing, rasping, sanding, ablating or frictional abrasion, i.e., bysliding the abrasive or cutting surface across the tissue to beresected. Impinging tissue to be targeted for abrasion may include, butis not limited to, lateral ligamentum flavum, anterior and medial facet,and osteophytes. The medical practitioner controls the force and speedof the abrasive surface against the tissue to be removed, while optionalcovers define the tissue exposed to the abrasive element.

One variation of the abrasive element cover envelopes the abrasivesurface and the backside of the belt or ribbon in areas where tissueremoval is not intended. A nerve stimulator may be incorporated into thetissue removal surface and/or the protective cover or sleeve in order toverify correct placement and enhance safety by allowing the medicalpractitioner to ensure that neural tissue is not subject to inadvertenttrauma or abrasion during the procedure.

The present invention also describes methods and apparatus that may beused as a compression dressing, after tissue resection or ablation.Following neuroforaminal and lateral recess enlargement, one variationof the compression dressing is placed in a position where it is firmlywrapped against the abraded tissue surface around the facet andligamentum flavum through the neural foramina. By tightly pressingagainst treated tissue surfaces, such a device serves to promote desiredtissue remodeling; to prevent edema that may lead to impingement onneural or vascular tissue during early healing; to contain debris; topromote postoperative hemostasis; to block scar formation between theraw tissue surfaces and the adjacent neural and vascular structures; toavoid inflammation or irritation to neural and vascular structures fromcontact with adjacent resected tissue surfaces; and as a mechanism forsustained drug delivery, possibly as a depot, to the operative sitepost-operatively (e.g. steroids, procoagulants, adhesion barriers).Finally, the dressing would also present a smooth surface towards thenerve root during the immediate post-operative period.

This neuroforaminal compression dressing may, for example, comprise theoptional protective sheath, percutaneously held tightly in place againstthe abraded surface. Alternatively or additionally, a separatepercutaneously removable compression dressing may be placed followingtissue abrasion, with or without a biodegradable component. In a furtheralternative embodiment, an entirely biodegradable compression dressingmay be placed tightly against the abraded surface, with the compressiondressing remaining completely implanted following the procedure.

Safe tissue removal, ablation and remodeling with these methods anddevices are further enabled by complementary methods and apparatusesthat assist with accurate neural localization. Neural localization willbe performed by neural stimulation through electrically conductivematerials located within the capped epidural needle tip; within theepidural tools that will be in contact with tissue to be modified; orone or both sides of the working barrier. Neural stimulation will beperformed in conjunction with monitoring of the patient for sensoryand/or motor response to the electrical impulses.

Said backstop may also contain neural localization capabilities,including a conductive element on the working side and/or thenon-working side. The conductive element may be used to ensure that theneural and their adjacent vascular structures are on the non-workingside of the barrier. In the instance that the barrier is placed throughthe lateral recess or neural foramina, appropriate low intensityelectrical stimulation on the non-working surface should result in thestimulation of sensory or motor nerves in the patient's extremity, whileappropriate electrical conduction on the working surface should resultin no neural stimulation. Neural stimulation may be monitored bymonitoring somatosensory-evoked potentials (SSEPs), motor-evokedpotentials (MEPs), and/or by looking for visual signs of muscularcontraction within the extremities. (Somatosensory evoked potentials(SSEPs) are non-invasive studies performed by repetitive, sub-maximal,electrical stimulation of a sensory or mixed sensory and motor nerve. Inresponse to the nerve stimulation the brain generates cerebral actionpotentials (electrical waves), that can be measured and recorded overthe scalp and spine with surface electrodes. In many cases, needleelectrodes are used for intraoperative SSEP monitoring, as they requireless current, and reduce artifact. The recorded response is a series ofwaves that reflect activation of neural structures.) SSEP, SEP, MEP orEMG feedback may be monitored and/or recorded visually, or may bemonitored audibly, potentially conveying quantitative feedback relatedto the volume or frequency of the auditory signal (e.g., a Geigercounter type of quantitative auditory feedback). Intensity of signal orstimulation may be monitored and used to localize the nerve duringplacement, as well.

For example, the surgeon may use the neural stimulator to ensure thatthere is not stimulation of vulnerable neurons on the working side ofthe barrier, prior to initiating tissue manipulation with the workingtools. For example, with the barrier in position in the lateral recessor neural foramina, the surgeon may send electrical current first alongthe working side of the barrier, then along the backside of the barrier.Low level stimulation of the working side would be expected to result inno neural stimulation, while the same stimulation on the backside of thebarrier would be expected to stimulate dorsal roots, nerve roots, organglia.

Neural localization may be further enabled by the addition of surgicalinstruments (e.g. cautery devices, graspers, shavers, burrs, probes,etc.) that are able to selectively stimulate electrically whilemonitoring nerve stimulation in similar fashions. Quantification ofstimulation may enable neural localization. For instance, one might usea calibrated sensor input that recognizes stronger stimulation as thedevice is closer the neural structures. For added safety, a surgicaldevice may be designed to automatically stimulate before or duringresection, and may even be designed to automatically stop resection whennerve stimulation has been sensed.

A method for modifying spinal anatomy is disclosed. The method includesdelivering a surgical apparatus to an epidural space and surgicallyaltering tissues that impinge neural or vascular structures in thelateral recess, neural foramina or central canal of the spine with theapparatus. Surgically altering tissues can include ablating tissue,resecting tissue, removing tissue, abrading tissue, retracting tissue,stenting tissue, retaining tissue, or thermally shrinking tissue.Surgically altering tissues can additionally include enlarging thelateral recess, neural foramina or central canal of the spine.

Delivering the surgical apparatus to an epidural space can includedelivering an epidural needle to the epidural space, and enlarging thelateral recess, neural foramina or central canal of the spine caninclude focally altering tissue with tools delivered through theepidural needle. Delivering the surgical apparatus to an epidural spacealso can include delivering an epidural needle to the epidural space,and enlarging the lateral recess, neural foramina or central canal ofthe spine also can include focally altering tissue with tools deliveredthrough a working channel disposed adjacent to the epidural needle.

Delivering the surgical apparatus can include converting the epiduralneedle to an endoscope within the epidural space. Delivering thesurgical apparatus to an epidural space also can include delivering aworking endoscope to the epidural space, and enlarging the lateralrecess, neural foramina or central canal of the spine can also includefocally altering tissue with tools delivered through the workingendoscope. Delivering the surgical apparatus can also include convertingthe epidural needle into a blunt tipped instrument after placement ofthe needle's tip within the epidural space. Converting the epiduralneedle can also include threading an epidural catheter through theepidural needle into the epidural space, and covering the needle's tipwith an epidural needle cover delivered via the catheter.

Delivering the surgical apparatus can also include converting theepidural needle into an endoscope via a visualization element disposedwithin the epidural catheter. Delivering the surgical apparatus caninclude infusing fluid into the epidural space to improve visualization.Delivering the surgical apparatus can include inserting a removableworking channel alongside the surgical apparatus. Delivering thesurgical apparatus can include inserting a distal tip of a dual lumenedepidural needle into the epidural space and using at least one of thedual lumens as a working channel for the delivery of instruments intothe epidural space. Delivering the surgical apparatus can includeinserting an instrument chosen from the group consisting of a tissuecauterization tool, a tissue laser device, a radiofrequency deliverydevice, a ronguer, a tissue grasper, a tissue rasp, a probe, a bonedrill, a tissue shaver, a burr, a tissue sander and combinations thereofthrough the surgical apparatus.

Delivering the epidural needle can include inserting the epidural needleto a position with a tip of the needle in proximity to where treatmentwill be directed. Delivering the epidural needle can include insertingthe epidural needle at an interspace below the level of the spine wherethe treatment will be directed.

Delivering surgical apparatus can include delivering the apparatus viaan open surgical route. Delivering the epidural needle can includedelivering the needle via a posterior, interlaminar percutaneous route.Delivering the epidural needle can include delivering the needle via aposterior, translaminar, percutaneous route. Delivering the epiduralneedle can include delivering the needle via a posterior, midline,interspinous, percutaneous route. Delivering the epidural needle caninclude delivering the needle via a percutaneous route through theneural foramen from its lateral aspect. Enlarging can include placing amechanical barrier or backstop between tissue to be resected andadjacent neural or vascular structures. The barrier can be steerable.

The method of modifying the spinal anatomy can include confirming properplacement of the surgical apparatus. Confirming proper placement caninclude confirming proper placement with a nerve stimulator. Confirmingproper placement with a nerve stimulator further comprises confirmingproper placement with stimulation leads placed on a tissue remodelingside of the surgical apparatus. The method of modifying the spinalanatomy can include confirming proper placement of the surgicalapparatus or barrier with a nerve stimulator having stimulation leadsplaced on a tissue remodeling side of the barrier or on a back side ofthe barrier.

The method of modifying the spinal anatomy can include monitoring nervestimulation with the nerve stimulator via somatosensory evokedpotentials (SSEPs). The method of modifying the spinal anatomy caninclude monitoring nerve stimulation with the nerve stimulator via motorevoked potentials (MEPs). The method of modifying the spinal anatomy caninclude monitoring nerve stimulation with the nerve stimulator via motorevoked patient movement. The method of modifying the spinal anatomy caninclude monitoring nerve stimulation via verbal patient sensory responseto the nerve stimulator.

The method of modifying the spinal anatomy can include monitoringenlargement via imaging. The method of modifying the spinal anatomy caninclude surgically altering the tissues under fluoroscopic imaging, MRIimaging, CT imaging, ultrasound imaging, radiological imaging, surgicaltriangulation, infrared or RF surgical triangulation.

The method of modifying the spinal anatomy can include placing anelement that provides tissue compression of surgically remodeled tissueor bone surface in order to enlarge the neural pathway or foraminapost-surgical enlargement. The method of modifying the spinal anatomycan include placing an element that provides tissue compression andretention in order to remodel tissue or bone surface in order to enlargethe neural pathway or foramina de novo. Placing the element can includeplacing the element using a percutaneous technique via the epiduralspace, through a neural foramen at a level to be treated for spinalstenosis, and around a facet complex or a lamina adjacent to the facetcomplex. The method of modifying the spinal anatomy can includetightening the element to a determined tension. Placing the element caninclude placing an element having a posterior anchor that is a cord ortie looped through a hole that has been drilled in the cephalad laminaof the immediately adjacent vertebrae. The method of modifying thespinal anatomy can include tensioning the element to a determined levelvia a tension gauge or other measurement device element holding tensionagainst the tissue to be remodeled.

The method of modifying the spinal anatomy can include releasing abiologically active material for the purposes of decreasinginflammation, or promoting remodeling of soft tissue or bone growth fromthe element.

Apparatus for focal tissue alteration are disclosed herein. Theapparatus have an element configured for placement into an epiduralspace, and surgical tools configured for delivery through the elementinto the epidural space to remodel spinal anatomy that impinges uponneural, neurovascular or tendon structures. The element can include anepidural needle, and wherein the surgical tools further comprise atissue remodeling device configured for placement via the epiduralneedle.

The epidural needle can be configured for placement into the epiduralspace via an approach chosen from the group consisting of a posteriorinterspinal midline approach, a posterior paramedian interlaminarapproach, a posterior translaminar paramedian approach through a hole inthe lamina, a neural foramina approach around an anterior border of afacet joint, and combinations thereof. The epidural needle can includetwo adjacent lumens, the second lumen configured to act as a workingchannel for the delivery of the surgical tools into the epidural space.

The apparatus can have an epidural catheter configured to convert theepidural needle into a blunt tipped instrument via an epidural needletip cover that may be opened and then pulled back to cover the needle'stip. The epidural catheter can have a fiberoptic cable forvisualization. The apparatus can have an insertable and removableworking channel for tool access configured for placement alongside theneedle.

The tissue remodeling device can be chosen from the group consisting ofa tissue cauterization tool, a tissue laser device, a radiofrequencydelivery device, a ronguer, a tissue grasper, a tissue rasp, a probe, abone drill, a tissue shaver, a burr, a tissue sander, and combinationsthereof.

The surgical tools can produce nerve stimulation. The apparatus can havea device for monitoring neural stimulation to identify when a workingsurface of the surgical tools is in close proximity to vulnerable neuraltissue during tissue remodeling.

An apparatus for protecting adjacent structures during remodeling ofspinal anatomy that impinges upon neural, neurovascular or tendonstructures is disclosed. The apparatus has a mechanical barrierconfigured for placement between tissue to be resected and the adjacentstructures. The mechanical barrier can be configured for insertionthrough an open incision. The mechanical barrier can be configured forinsertion through a working channel of an endoscope.

The apparatus can be configured for use with a visualization element.The visualization element can be chosen from the group consisting of anepidural endoscope, a fluoroscope, ultrasound, XRay, MRI andcombinations thereof. The apparatus can have a nerve stimulator tofacilitate proper placement of the barrier. A conductive element can beincluded on a tissue modification side of the barrier or on a backsideof the barrier to facilitate nerve localization. A working surface ofthe tissue remodeling device can have neurostimulation capabilities,thereby allowing for a positive and negative control in localizingneural tissue prior to tissue removal.

The apparatus can include a monitoring technique for monitoringelectrical nerve stimulation. The monitoring technique can be chosenfrom the group consisting of SSEPs (somatosensory evoked potentials);MEPs (motor evoked potentials); EMG; verbal inquiries of the patient'ssensory experience to the electrical stimulation; visual techniques,mechanical techniques, tactile techniques monitoring neuro muscularstimulation and movement, and combinations thereof.

The apparatus can include an element configured to provide tissuecompression against surgically remodeled tissue or bone surface in aneural pathway or foramina post-enlargement. The element is configuredfor percutaneous placement via the epidural space, through theneuroforamen at the level to be treated for spinal stenosis, and aroundthe facet complex or the lamina adjacent to the facet complex. Theelement is configured to release a biologically active material for thepurposes of decreasing inflammation, or promoting remodeling of softtissue or bone growth.

The apparatus can be configured for tightening to a determined tensionfor purposes of relieving spinal stenosis. The element can include aposterior anchor having a cord or tie looped through a hole that hasbeen drilled in the cephalad lamina of the immediately adjacentvertebrae. Tension of the element is configured to be set at adetermined level by a tension gauge, or other measurement device elementholding tension against tissue to be remodeled.

The apparatus can have a neuro foraminal compression element configuredto retract and hold pressure on spinal tissue when placed under tension,in order to relieve pressure on impinged neural and vascular structuresand promote tissue remodeling. The apparatus can have a tensioningdevice for the neuro foraminal compression element configured to securetwo ends of the element together at a posterior aspect of the vertebrallamina at a desired tension by pulling the element to the desired levelof tension prior to locking the opposite ends of the element together atsaid tension.

The apparatus can have a tensioning device configured to tighten a loopformed by the neuro foraminal compression element around the facet jointcomplex, within the lateral aspect of the lamina, and configured totighten the compression element across a locking or crimping element toa specified tension, pulling the ligamentum flavum posteriorly in thespinal canal, in the lateral recess and in the neural foramen.

The apparatus can have a tensioning device configured to tighten a loopformed by the neural foraminal compression element around the lamina,close to a facet joint complex, within a lateral aspect of the lamina,and configured to tighten the compression element across a locking orcrimping element to a specified tension, pulling the ligamentum flavumposteriorly in the spinal canal, in the lateral recess and in the neuralforamen.

At least one free end of the neural foraminal compression element can beconfigured for subcutaneous placement to facilitate future removal ofthe element. The compression element can be biodegradable.

The compression element can contain a therapeutic agent chosen from thegroup consisting of medications, bioactive compounds, steroids, depotsteroids, anti-inflammatories, and combinations thereof. The agent canbe configured for immediate release. The agent can be configured forsustained local delivery.

A method of altering bone or soft tissue in a patient is disclosed. Themethod includes placing a tissue abrasion device through tissue to bealtered, holding the tissue abrasion device under tension to bring anabrasive surface of the device firmly against the tissue to be altered,and sliding the abrasive surface of the abrasive element against thetissue to be altered, thereby altering bone or soft tissue immediatelyadjacent to the abrasive surface. Altering can include abrading,removing, or remodeling.

Placing the tissue abrasion device through tissue to be altered caninclude placing the device through spinal tissue that impinges onneural, neurovascular or ligamentous structures in the patient's spine.Placing the tissue abrasion device can include placing the tissueabrasion device through a neural, neurovascular, or ligamentous pathwaywithin the patient's spine, holding the tissue abrasion device undertension to bring the abrasive surface against tissue within the pathway,and where sliding includes enlarging the pathway via frictional abrasionof the tissue. Placing a tissue abrasion device through the pathway caninclude placing the tissue abrasion device through neural foramina ofthe patient's spine and around the anterior border of a facet joint.Placing the tissue abrasion device through neural foramina of thepatient's spine and around the anterior border of a facet joint caninclude placing the device via a route chosen from the group consistingof an open surgical approach, a percutaneous approach, a posteriorpercutaneous approach, an interlaminar percutaneous approach, atranslaminar percutaneous approach, an interspinous percutaneousapproach, through the neural foramen from a lateral direction, andcombinations thereof. Placing the tissue abrasion device can includeplacing the device within a protective sheath or cover.

The method can include altering spinal tissues that impinge on neural,neurovascular, or ligamentous structures in the patient's spine.

Enlarging the pathway can include enlarging a diseased pathway withinthe patient's spine.

Holding the tissue abrasion device under tension against tissue withinthe pathway can include placing an abrasive surface of the tissueabrasion device against tissue chosen from the group consisting of ananterior surface of facet joint capsule, a medial surface of facet jointcapsule, a superior articular process of the facet joint, ligamentumflavum, tissues attached to ligamentum flavum, extruded spinal discmaterial, scar tissue, and combinations thereof.

Sliding the tissue abrasion device against the tissue can includesliding the abrasive surface of the tissue abrasion device against thetissue. Sliding the abrasive surface can include enlarging the lateralrecess, neural foramina or central spinal canal via frictional abrasion.Sliding the abrasive surface can include preferentially abrading tissuechosen from the group consisting of ligamentum flavum, bone spurs, facetcapsule, superior articular process, extruded spinal disc material, scartissue and combinations thereof that impinge on neural or vascularstructures.

The method can include confirming proper placement of the tissueabrasion device. Confirming proper placement of the device can includeconfirming proper placement with a nerve stimulator. Confirming properplacement with a nerve stimulator can include confirming properplacement with a nerve stimulator having stimulation leads placed at alocation chosen from the group consisting of a non-abrasive side of thetissue abrasion device, a back side of a protective sleeve or coverplaced over the tissue abrasion device, an abrasive side of the tissueabrasion device, a working side of the tissue abrasion device, andcombinations thereof. Confirming proper placement can include confirmingplacement via a modality chosen from the group consisting offluoroscopic, MRI, CT, infrared, ultrasound imaging, surgicaltriangulation, and combinations thereof.

The method can include monitoring nerve stimulation viasomatosensory-evoked potentials (SSEPs) with the nerve stimulator. Themethod can include monitoring nerve stimulation via motor-evokedpotentials (MEPs) with the nerve stimulator. The method can includemonitoring nerve stimulation via verbal patient sensory response to thenerve stimulator.

The method can include replacing the tissue abrasion device with acompression element that is held against altered tissue or bone.

Apparatus for the removal of impinging soft tissue or bone within apatient are disclosed. The apparatus can have a tissue abrasion deviceconfigured for placement through impinged tissue pathways. The tissueabrasion device can have an abrasive surface configured for placementadjacent to the impinging tissue. The impinged tissue pathways can havepathways chosen from the group consisting of neural pathways,neurovascular pathways, ligamentous pathways, and combinations thereof.The tissue abrasion device can be configured for the removal of spinalstructures that impinge neural or neurovascular tissues within thepatient, and wherein the tissue abrasion device is configured forplacement through neural foramina of the patient's spine and around theanterior border of a facet joint.

The apparatus can have a protective cover disposed about the tissueabrasion device, where the protective cover is configured to limitexposure of an abrasive surface of the device to areas where tissueremoval is desired. The apparatus can have a nerve stimulator incommunication with the tissue abrasion device to facilitate properplacement of the device.

The apparatus can have a conductive element disposed on an abrasivesurface of the device to enable nerve localization by sending a smallelectrical current through the conductive element.

The apparatus can have an epidural needle, where the tissue abrasiondevice is configured for placement through the epidural needle.

The apparatus can have a visualization element for direct visualizationof the neural foramina. The apparatus can have a neural foraminacompression element.

The compression element can be configured to promote hemostasis anddesired tissue remodeling during healing. The element can be configuredto be left in place after being secured with adequate tension againsttissue abraded with the tissue abrasion device. The compression elementcan be configured to protect a tissue surface abraded with the device.The compression element can be configured to prevent adhesions duringhealing. The compression element can be configured to protect vulnerablestructures adjacent to tissue abraded with the tissue abrasion devicefrom an inflammatory response triggered by tissue abrasion.

The tissue abrasion device can be configured for placement in front of,across, and then behind tissue to be abraded, such as through anaturally occurring or artificially created anatomical foramen or tissuepathway. The abrasive surface can be disposed on all or part of one sideof the tissue abrasion device. The abrasive surface can be disposed onan element chosen from the group consisting of a length of ribbon,strap, cable, belt, cord, string, suture, wire and combinations thereof.The ends of the device can be configured for manual grasping. Theapparatus can have a handle to which ends of the device are attached formanual grasping. The device can be configured for attachment to anelectromechanical power-driven device.

The device can be configured to be placed under tension in order tobring the abrasive surface into contact with tissue to be removed. Theabrasive surface can be configured to be pulled against tissue to beremoved. The abrasive device can have multiple abrasive elements withdifferent abrasive surfaces, configured for interchangeable use. Themultiple abrasive elements can have varying grades of abrasive material.The multiple abrasive elements can have different grooves, patterns ofgrooves, or material patterns on the abrasive surface to facilitatepreferential abrasion of tissue at desired locations. The patterns ofgrooves can have diagonal parallel grooves that preferentially move theabrasive element towards one direction on the surface being abraded asthe abrasive element is pulled in one direction, and towards an opposingdirection as the abrasive element is pulled in a second direction. Themultiple abrasive elements can have different shapes that guide theextent and location of tissue removal.

The apparatus can be configured to carry debris away from the site oftissue removal.

The tissue abrasion device can vary in profile along its length. Thetissue abrasion device can have openings that facilitate passage ofdebris behind the device for storage or removal.

The apparatus can have a monitor for monitoring electrical nervestimulation with the nerve stimulator. The monitor can be configured tomonitor a feedback chosen from the group consisting of SSEPs, MEPs, EMG,verbal communication of patient sensation, visual monitoring, mechanicalmonitoring, tactile means, monitoring of neuromuscular stimulation andmovement, and combinations thereof.

The compression element can be biodegradable. The compression elementcan contain a therapeutic agent configured for delivery to abradedtissue or adjacent neural and neurovascular structures. The therapeuticagent can be a medication, bioactive compound, steroid, depot steroid,anti-inflammatory, adhesion barrier, procoagulant compound, orcombination thereof.

The protective cover can be attached, external to the patient, to asuspension system that includes elements to firmly and individuallygrasp each end of the cover and hold it in position under tensionagainst the tissue surface to be abraded, with an open portion of thecover exposing the abrasive element directly over tissue to be abraded.The protective cover can be configured to protect a non-abrasive side ofthe tissue abrasion device. The protective cover can have channels alongits lateral aspects for the insertion and sliding of the tissue abrasiondevice. The protective cover can include channels along its lateralaspects for the insertion and sliding of a second protective coverconfigured for placement between an abrasive surface of the tissueabrasion device, and tissue adjacent to tissue to be abraded with theabrasive surface.

Finally, the present invention also describes methods and apparatus thatpromote tissue remodeling, separate from the tissue resection orablation. These devices tightly wrap, retract, or hold in position,under tension, impinging tissues within the spinous posterior elements.

It is expected that the apparatus and methods of the present inventionwill facilitate a minimally invasive approach to the selectiveelimination of pathological spinal tissue, thereby enabling symptomaticrelief in patients suffering from spinal stenosis.

BRIEF DESCRIPTION OF THE DRAWINGS

The above and other objects and advantages of the present invention willbe apparent upon consideration of the following detailed description,taken in conjunction with the accompanying drawings, in which likereference characters refer to like parts throughout, and in which:

FIG. 1 is a cross section through the posterior aspect of the lumbarspine;

FIG. 2 is a sagittal section through the lumbar spine;

FIGS. 3 a, b, c are sagittal views through a patient's spine,illustrating a prior art method for epidural needle insertion, a loss ofresistance method;

FIG. 3 a illustrates a needle inserted to an interspinal ligament.

FIG. 3 b illustrates constant pressure applied on the syringe plunger.

FIG. 3 c illustrates saline injected into the epidural space.

FIG. 4 is a cross-sectional view through a patient's spine, illustratingtwo prior art variations of the method of FIGS. 3 a, b, c;

FIG. 5 is an illustration of standard Touhy epidural needle tips;

FIG. 6 are schematic side views illustrating a method and apparatus, inaccordance with the present invention, for covering with a cap andblunting the sharp tip of an epidural needle post-insertion;

FIG. 7 are also a schematic side view of variations of the apparatus ofFIG. 6 with a method for also limiting the depth of insertion ofcannula, access portal, or needle;

FIG. 8 are schematic side views illustrating a method and apparatus inaccordance with the present invention for covering with a cap andblunting the tip of the epidural needle post-insertion, and optionallyconverting the epidural needle to an epidural endoscope, for safefurther advancement of the needle into the epidural space;

FIG. 9 are also a schematic side view of variations of the apparatus ofFIG. 8;

FIG. 10 are also a schematic side view of variations of the apparatus ofFIG. 6 or 8;

FIG. 11 are also a schematic side view of variations of the apparatus ofFIG. 8;

FIGS. 12 a, b, c are schematic side views of variations of the apparatusof FIG. 6 or 8;

FIGS. 12 d, e are schematic side views of an epidural portal over needleapparatus, as shown in FIGS. 12 a, b, c; with a distal anchor engagedanterior to the ligamentum flavum, when the portal has been insertedover the needle, into the epidural space;

FIG. 13 is a schematic side view of variations of the apparatus of FIG.6 or 8;

FIG. 14 a is a schematic side view, partially in section, of variationsof the apparatus, illustrating methods of safely utilizing the apparatus(e.g., safe tool access) for safe placement and use of surgical tools inor around the epidural space;

FIG. 14 b are side views, partially in section, illustrating a methodand apparatuses for safe placement of a tool or working channel into theepidural space;

FIG. 15 are side views illustrating apparatuses that include a doublebarreled epidural needle, with the epidural needle as the most distalpoint, and with the working channel the more proximal tip. This systemmay also be converted to an endoscope and may be used for safe placementof instruments into the epidural space;

FIGS. 16-18 are cross-sectional views through a patient's spine,illustrating a method and apparatus for placement of a double barreledepidural needle or endoscope, the sharp tip of which has been covered inFIG. 17, and thereby blunted, for safe advancement towards the lateralrecess and neural foramina. The blunted epidural needle apparatus maycontain a fiberoptic cable for direct visualization, in a preferredembodiment;

FIG. 19 is a cross-sectional view through a patient's spine thatillustrates a method, following FIGS. 16-18, for placement of a workingbackstop or barrier into the lateral recess and/or neural foramina. Thebarrier or backstop may contain elements for neural localization;

FIGS. 20-21 are cross-sectional views through a patient's spine thatillustrate alternative methods and apparatuses for placement of aworking backstop or barrier to enable safe tissue resection, ablation,abrasion or remodeling;

FIG. 22 is a cross-sectional view through a patient's spine thatillustrates a tool inserted through the working channel (example shows ashaver or burr), with its tip in position for tissue removal ordebridement, adjacent to a protective working backstop or barrier.

FIG. 23 are schematic views of a working backstop or barrier apparatus,including an optional rail for controlled tool placement in relation tothe barrier, and an optional conductive element for neural localization.

FIG. 23 b is a frontal view from above;

FIG. 23 c is a front view;

FIG. 23 d is a frontal view of the working backstop or barrier apparatusfolded for compact delivery;

FIG. 24 is a cross-sectional view through a patient's spine thatillustrates a methods and apparatuses for providing neural stimulationand neural localization, within a working backstop or barrier, and/orwithin a tool (a bone burr placed adjacent to a spinal bone spur in thelateral recess, in this illustrative example), for safety in tissueresection, abrasion or remodeling;

FIGS. 25-32 are cross-sectional views through a patient's spine,illustrating a method and apparatus for placement and use of elementsfor selective surgical removal of tissue;

FIGS. 33-36 are cross-sectional views through a patient's spine,illustrating a variation of the method and apparatus of FIGS. 25-32;

FIGS. 37 a-d are cross-sectional views through a patient's spine,illustrating another variation of the method and apparatus of FIGS.25-32;

FIG. 38 are a detailed view and a close up of the cross section of apreferred embodiment of the apparatus used in FIG. 37 d;

FIG. 39 an alternative embodiment of the apparatus of FIG. 38;

FIGS. 40-45 are partial cross-sectional views through a patient's spine,illustrating a method for use with single or multiple lumen deliverysystems, for placement of an abrasion apparatus through the neuralforamina for selective surgical removal of tissue;

FIGS. 46-58 are cross-sectional views through a patient's spine,illustrating a variation of the methods and apparatus of FIGS. 40-45,which may also be used with single or multiple lumen delivery systems;

FIG. 59 is a cross-sectional view through a patient's spine,illustrating a methods and apparatus that, under tension, anchors andsuspends the working sheath or protective sleeve that covers theneuroforaminal abrasion device;

FIG. 60 is a cross-sectional view through a patient's spine,illustrating a method and apparatus that, under tension, provides apercutaneous compression dressing over the abraded area. In thisillustration, the compression dressing is the same working sheath orprotective sleeve that had covered the neuroforaminal abrasion device;

FIG. 61 is a schematic cross-sectional view through a patient's spine,illustrating a method and apparatus for achieving neural localizationprior to or during use of the tissue removal apparatus;

FIG. 62 are schematic views of additional apparatus, showing a spool orreel to reel configuration of a portion of the device that may beutilized for selective surgical removal of tissue;

FIGS. 63-70 are schematic cross-sectional views through a patient'sspine of a method and apparatus for a posterior midline or paramedianapproach to placement of a posterior elements compression, retraction orretention device around the facet complex, through the neural foramina;

FIG. 71 are schematic cross-sectional views through a patient's spineillustrating a posterior lateral approach to placement of the spinalcompression, retraction or retention apparatuses;

FIG. 72 are schematic cross-sectional views through a patient's spine ofa fully implanted compression or retraction remodeling apparatus orcompression dressing apparatus;

FIG. 73 is a schematic cross-sectional view through a patient's spine ofan apparatuses for a compression remodeling strap integrated with aworking backstop or barrier.

FIG. 74 is a cross-sectional view through a patient's spine that shows afacet drill with a ligament retraction device around a working backstop,and demonstrates a image guided drill used in conjunction with thebackstop;

FIGS. 75-78 are schematic views of cable strap configurations fortemporary removable, permanent, or biodegradable compression dressingsor remodeling tools;

FIGS. 79-80 are schematic cross-sectional and lateral views through #patient's spine of apparatuses for temporary or permanent retraction andretention of the ligamentum flavum;

FIG. 81 are sagittal cryosection images through 3 cadaveric spines(images courtesy of Wolfgang Rauschning, Md.) that illustratepathological anterior bulging and “buckling” of the ligamentum flavum,encroaching on the spinal canal or lateral recess, a frequentcontributing factor in spinal stenosis. In circumstances when similarlyprotruding ligamentum flavum impinges neural and neurovascularstructures in the spinal canal, lateral recess, or neural foramina, thenretraction of said ligaments, as in FIGS. 79 and 80 may be beneficial tothe patient;

FIG. 82 are cross-sectional views through a protective sleeve or sheath,compact during insertion (b), and expanded (c) by passing the apparatusthrough its lumen;

FIG. 83 are schematic cross section views of additional apparatus thatmay be utilized for selective surgical removal of tissue;

FIG. 84 are schematic cross section views of additional apparatus thatmay be utilized for selective surgical removal of tissue, andsubsequently as a compression dressing, with the ability to act as atherapeutic drug depot;

FIG. 85 are schematic cross section views of additional apparatus thatmay be utilized for selective surgical removal of tissue;

FIG. 86 is a schematic cross section views of additional apparatus thatmay be utilized for selective surgical removal of tissue;

FIG. 87 are close-up schematic views of the resecting element in FIG. 86that may be utilized for selective surgical removal of tissue;

FIGS. 88-93 are schematic lateral views of additional apparatus that maybe utilized for visualization in the epidural space, enabling theselective surgical removal of tissue;

FIG. 88 illustrate an embodiment of an endoscope in a clear tippedcannula;

FIG. 89 illustrate an embodiment of a 0-degree endoscope rotated inunison with a curved, clear tipped cannula;

FIG. 90 illustrate an embodiment of a 30-degree endoscope rotatedseparately inside of a clear tipped cannula;

FIGS. 91 a-c illustrate various embodiments of a clear tipped cannulawith a clear shaft;

FIGS. 91 d-f illustrate various embodiments of a clear tipped cannulawith an opaque shaft;

FIG. 92 illustrate an embodiment of a clear tipped cannula with aflexible neck;

FIG. 93 illustrates an embodiment of an endoscope with a built-in clearcover (e.g., a combination device embodiment);

FIGS. 94-99 are schematic lateral views of similar apparatus forvisualization in the epidural space, along with additional method andapparatus that enable the safe placement and use of tools for selectivesurgical ablation, resection, abrasion and remodeling of tissue;

FIG. 94 illustrate various embodiments of a clear tipped cannula with afree adjacent tool;

FIG. 95 illustrate various embodiments of a clear tipped cannula with anattached adjacent tool;

FIG. 96 a illustrates an embodiment of a clear tipped cannula with aworking channel for a tool;

FIG. 96 b illustrates an embodiment of a clear tipped cannula with anerve stimulator at a working channel exit;

FIG. 97 illustrate various embodiments of cannulas with a nervestimulator at the tip (e.g., EMG sensors peripherally placed);

FIG. 98 illustrate various embodiments of a clear tipped cannula with anerve stimulator at a tip of the free tool; and

FIG. 99 illustrate various embodiments of a clear tipped cannula with anerve stimulator at a tip of the free or attached tool.

DETAILED DESCRIPTION

The present invention relates to methods and apparatus for the selectivesurgical removal or alteration of tissue that impinges upon spinalneural or vascular structures, with particular attention towardsavoiding injury to the affected or adjacent neural and neurovascularstructures. More particularly, a preferred embodiment of the presentinvention relates to methods and apparatus for lateral recess 108 andneural foraminal enlargement of the spine, in cases of neurovascularimpingement, through a novel approach to selective and safe enlargementof the pathologically narrow spinal neural foramen 110, impinged lateralrecess 108 and/or compromised central spinal canal. Tissues that impingethe spine's central canal, lateral recess 108, and neural foramen 110may include, but are not limited to, ligamentum flavum 10; bone spurs orligamentous calcifications; localized disc extrusions; enlarged facetjoint complex 12, facet capsule, and superior articular processes; andscar tissue or adhesions.

The variations of the invention designed to treat spinal stenosis aresummarized in this paragraph, and described in greater detail in theparagraphs that follow. The methods begin with insertion of an epiduralneedle 2 apparatus, which is converted, after placement in the epiduralspace, from a sharp tipped instrument, into a blunt tipped tool. Theblunt tool is manipulated within the epidural space. Accurate toolmanipulation may be facilitated with the use of image guidance; directvision via an accompanying epidural endoscope; or direct vision when theinstrument itself is given endoscopic function. The same blunt tippedepidural instrument may have an attached fixed or removable workingchannel. An additional apparatus of the current invention, a workingbackstop or barrier 96 that serves to protect adjacent vulnerablestructures during the procedure, may subsequently be inserted into theepidural space, as well as through the neural foramina, through theneedle or endoscope or an adjacent working channel. Safe resection,ablation, and remodeling may be further ensured through integration intothe invention of electrical neural stimulation and monitoring forlocalization, optionally available through nerve stimulationfunctionality in the epidural instrument; in the working tools usedthrough the needle or working channel; and/or in either or both sides ofthe working backstop 96. Finally, further variations of the device andmethod enable the surgeon to remodel stenotic spinal anatomy, eitherafter tissue resection, cutting, or abrasion or as stand-aloneprocedures, through the placement of devices for holding, retracting orretaining anatomic structures away from vulnerable neural andneurovascular structures within the posterior elements of the spine.

FIG. 1 shows the posterior elements of the spine in axial cross section.The epidural space 42 in the spine is consistently more accessible inits posterior most aspect, a fat filled zone most popular for safeepidural needle 2 placement, posterior to the dura mater 46. The dura 46covers and contains the central neural elements of the spine, includingthe spinal cord, cauda equina 140, nerve roots 62, and spinal fluid.FIG. 2 illustrates the spine in sagittal section. FIGS. 1 and 2 show twoof the most important anatomic structures involved in the impingement ofneural and neurovascular tissue in spinal stenosis—the ligamentum flavum10 and the facet joint complex 12. FIG. 2 illustrates spinous processes80.

For posterior approaches to the lateral recess 108 and neural foramen110, the needle 2 is inserted at or one level below the spinalinterspace where tissue abrasion and removal is desired. The epiduralneedle 2 may be inserted into the epidural space 42, midline,ipsilateral, or contralateral to the area where the spinal canal,lateral recess 108 and/or neuroforaminal stenosis or impingement is tobe treated. Referring now to FIG. 3, a prior art method for epiduralneedle 2 insertion is shown, comprising a standard loss-of-resistancetechnique. Needle based device placement may be approached from eitherthe medial or the lateral side of the neural foramen 110. FIG. 3illustrate a midline interspinous approach to the posterior epiduralspace 42. Using this technique, a large bore (e.g. 12 to 18 gauge)epidural needle 2 is inserted into interspinal ligaments, and isdirected towards the posterior epidural space 42, while fluid (e.g.sterile saline) or air is compressed within the syringe 60, meetingresistance to injection. Upon entry of the needle tip into the epiduralspace 42, perhaps through the ligamentum flavum 10, there is a manuallyperceptible “loss of resistance” to the continued pressure on theplunger of the syringe 60, as the compressed fluid or air easily entersthe epidural space 42, without resistance, signifying correct needle tipposition (i.e., placement). The epidural space has a slight negativepressure.

Alternative posterior epidural needle 2 entry approaches into theepidural space are illustrated in FIG. 4, including interlaminarparamedian and midline interspinous techniques, a preferred approach tothe medial side of the neural foramen 110. An alternative posteriortranslaminar approach, where the needle is placed through a hole in thelamina 122 [LA], is not shown. The epidural space may also be enteredvia a more lateral, neuroforaminal approach to needle placement, asshown in FIG. 71. With any percutaneous epidural approach, after asterile prep and drape, the epidural needle's 2 sharp tip is insertedthrough the skin to perform a loss-of-resistance technique.

When a midline approach is used, the epidural needle's 2 sharp tip isinserted through the skin until it begins to engage the interspinousligaments 78. Subsequently, a fluid or air filled (loss of resistance)syringe 60 is depressed and will meet resistance to injection, until theneedle tip is advanced, through the ligamentum flavum 10, entering theepidural space 42, which actually has a slight negative pressure. Thereis a clear “loss of resistance” to the pressurized contents of thesyringe 60, which occurs upon entering the epidural space 42, signifyingcorrect needle tip placement.

When interlaminar access is not possible (e.g. unusual cases whenlaminae 122 are too tightly approximated, even with flexion of theback), the epidural space may be entered via a translaminar burr hole,using a drill 176 (e.g., an image guided drill) designed for safeepidural entry. Each of these approaches allows placement of theepidural needle 2 tip in the posterior epidural space 42, poised foraccess to the lateral recess 108 and neural foramen 110.

After the epidural needle's distal tip has been placed in the posteriorepidural space 42, a specially designed epidural catheter 24 is threadedthrough the needle 2. Once threaded into the epidural space 42, theepidural catheter's unique epidural needle tip cap or cover 36, locatedin the distal end of the epidural catheter 24 (with needle tip coveringcapabilities) is opened and pulled back to cover the sharp epiduralneedle 2 tip, locked in place, and thereby converts the needle to anon-sharp (e.g., blunt) instrument. The needle, thus converted, may bemanipulated and more safely advanced in the epidural space. The bluntedneedle is subsequently advanced in a direction parallel to the dura 46,in a gentle manner, taking care to avoid inadvertent dural, neural orvascular trauma. With reference to FIGS. 6, 8, 9, 10, 11, 12, and 13,methods and apparatus for protecting, covering and blunting the sharptip of the epidural needle 2 post-insertion, and optionally convertingthe epidural needle 2 to an epidural endoscope 132, are described. Thecatheter apparatus 24 is inserted through the needle, and into theepidural space 42, as in FIGS. 6 b, 8 b, 9 a, 10 b, 11 b, 12 a, and 13c. The catheter tip may be converted to the open position by one ofseveral mechanisms, for example, the catheter illustrated in FIG. 9 hasa port 34 for injection of air or liquid to the open the epidural needletip cover. The injected air or liquid drives (e.g., opens) the actuatorfor the catheter's tip (needle cover). By forcing air or fluid into port34 in the epidural catheter 24, a portion of the catheter's tip 36 maybe expanded, as in FIGS. 6 b, 8 c, 9 b, 11 c, 12 b, or 13 e, to inflateor otherwise open the needle's protective cover or cap 36. In anothervariation, an alternative means of actuation of the cap system on theepidural catheter 24 may be a wire or string that pulls the cap into anew shape. For example, FIG. 12 demonstrate a sliding umbrella-likemechanism for actuation of the distal epidural catheter 24 based needletip cover 36. FIG. 9B shows the epidural “needle cap” or “fiber cap” 36in the opened position. In certain embodiments, the catheter may nextneed to be pulled back proximally through the needle 2 until, as in FIG.9C, until the epidural needle cover 36 is engaged over the distal needletip, protecting the dura 46, neural and vascular structures from thesharp point of the needle 2, which is no longer exposed. Markings on thecatheter may be used to demonstrate to the surgeon that the catheter isin the correct position, allowing the blunted epidural instrument to besafely advanced.

Once the tip of the epidural needle 2 has been blunted or capped, and nolonger has a sharp exposed portion, the needle may be safely advancedwithin the epidural space, preferably in a direction parallel to thedura 46 (FIG. 13). In one variation, the epidural needle 2 tip iscovered by the catheter based device, then is advanced through theepidural space under image guidance (e.g. fluoroscopy, CT, x-ray, MRI,Ultrasound, etc.), towards the area where tissue resection, ablation orremodeling is to be performed.

In an alternative variation of the method and device, as in FIGS. 8, 9,11, and 13, the epidural catheter 24, in addition to a needle tip cover,also contains a fiberoptic cable 38 (or clear cover over the distal endof the fiberoptic cable within the epidural catheter), which enablesconversion of the epidural needle 2 into an epidural endoscope 132. Thefiberoptic component 38 of the catheter provides the surgeon with anability to directly visualize the epidural space 42. In a furthervariation of the method, both fiberoptic visualization and imageguidance may be used concurrently.

In this apparatus and method for enabling safe manipulation of theapparatus in the epidural space, an epidural needle 2 is first placed inthe posterior epidural space 42 in a similar manner to what wasdescribed above. With the needle tip in the epidural space 42, anepidural catheter 24 apparatus is used to deliver a cover to the sharpepidural needle 2 tip, converting the needle to a blunt instrument forfurther atraumatic advancement of the apparatus into the epidural space,as shown in FIGS. 6, 9, 11, and 12. After the catheter 24 is advancedthrough the epidural needle 2 into the epidural space 42, as in FIGS. 6a and 9 a, a distal portion of the catheter is converted to a shape thatwill be used to cover the sharp epidural needle 2 tip, as illustrated inFIG. 6 b.

Once the cover 36 in the distal catheter 24 is opened, the catheter 24is gently pulled back until the needle tip is covered and therebyblunted. The capped needle is next carefully advanced within theepidural space 42, between the ligamentum flavum 10 and the dura 46,somewhat parallel to both, towards one of the neural foramen 110, withmuch less risk of inadvertent dural puncture. In order to furtherfacilitate safe advancement of the capped needle in the epidural space,image guidance may be used. Additionally or alternatively, the epiduralneedle 2 may be converted to an epidural endoscope. Conversion to anendoscope may be performed by either converting the epidural needle 2 toan endoscope directly (“needlescope”), or by utilizing the epiduralneedle 2 to enable placement of an endoscope cannula or portal 56, whichwill replace the needle 2. The needle 2 may be converted to an endoscopedirectly through use of the catheter 24 that is used to cover, blunt, or“safe” the epidural needle 2 tip. The epidural catheter 24 optionallymay contain a rigid or flexible fiberoptic element 38, through which thesurgeon may view the epidural space 42, thereby converting the epiduralneedle 2 into an epidural endoscope. The tip of the fiberoptic catheterwould, in such a case, be clear 38.

FIG. 7 illustrates a distal epidural anchor 40. The distal epiduralportal anchor 40 can, in its engaged position, hold the distal portionof the epidural apparatus in the epidural space, anterior to theligamentum flavum. FIG. 7 also illustrates that the portal, needle, orendoscope may include a proximal epidural anchor, stopper or lock 28(e.g., to anchor on the skin) that may be advanced from the proximal endof the device (skin side), in order to help to prevent the percutaneousdevice from advancing further into the epidural space than is desired(as in FIG. 7 b). The lock 28 can be inserted over the portal andagainst the skin when the portal is at a desired depth.

In a further variation of the apparatus and method, an epidural portal56 would allow interchangeable epidural endoscopes to be used to view orwork within the epidural space. An epidural needle 2 may be used toplace an endoscope portal 56, using one of the three following generalapproaches: (a) In one variation, a portal is an expandable catheter(e.g. FIG. 82) that is delivered as a catheter through the epiduralneedle 2; (b) In another preferred embodiment, an epidural needle 2 maybe inserted into the epidural space, with a thin walled epidural cannulaor portal 56 already in place over it, similar to the method andapparatus of standard intravenous cannulation with IV catheters usedtoday. This technique would ideally be used in conjunction with theepidural needle 2 method and apparatus, so that the needle may beadvanced far enough to safely also place the neck of the cannula orportal 56, which is a short distance proximal to the distal tip of theepidural needle 2, into the epidural space. In order be able to safelyadvance the portal 56 into the epidural space, the needle may be coveredor blunted, as described above, using a catheter that does not contain afiberoptic element, as in FIG. 6. With the sharp tip covered, the needlemay be subsequently advanced a few millimeters, until the distal tip ofthe portal has also been advanced into the epidural space 42; (c) In athird embodiment of the method and apparatus, the portal 56 may beinserted over a soft tipped flexible guidewire that has been placedthrough the epidural needle 2, analogous to the popular “SeldingerTechnique” (a standard cannula over needle insertion approach tovascular access).

With reference to FIG. 14, additional variations of the apparatus ofFIG. 9 are described, illustrating methods of safely utilizing theapparatus, in combination with additional surgical tools. Safe toolaccess, for example, may be facilitated by the inclusion of either aworking channel 50 on an epidural endoscope, or by sliding the toolalong a rail 52 and slot 58 interface on the epidural cannula or“needlescope” 56. FIG. 14A shows tool 54 (illustratively a grasper)fitted with rail 52 that mates with a slot 58 of epidural endoscope, sothat it may be inserted directly into the epidural space 42 and placedin the “safe zone”, without the need for a working channel alongendoscope/needle.

In FIG. 14B, working channel 50 is disposed along epidural needle 2,“needlescope”, or endoscope, e.g., is integrally formed with theendoscope or is positioned via a rail and slot mating, or a similarremovable fastening mechanism, with the endoscope. FIG. 14B illustratesan epidural working channel 50 in place, connected to the cannula,needle, or endoscope, with its tool-presenting end adjacent to the “safezone”.

In order to further facilitate working in the epidural space 42, theepidural portal or cannula 56 may have, preferably close to its distaltip, an anchor system 40 to prevent said apparatus from inadvertentlyslipping out of the epidural space 42, as illustrated in FIG. 7. Theanchor 40 may be engaged towards the distal tip of the cannula or portal56, anterior to the ligamentum flavum 10. The portal 56 may also beanchored external to the epidural space 42, e.g., to the patient's skin70 (e.g., of the patient's back), or within interspinous 78 orsupraspinous ligaments.

Referring now to FIG. 15, an additional method and apparatus forplacement of the tissue modification elements is illustrated. A twin(i.e., double) lumen epidural needle 84 is illustrated, comprising aworking channel 50 adjacent to the epidural needle 2. The second lumenserves as a working channel 50, or for the delivery of tools into oradjacent to the epidural space 42. Note that the distal beveled apertureof the working channel is proximal to the epidural needle 2 tip, andopens onto the side of the epidural needle 2 that the epidural bevelfaces. The double lumen epidural needle 84 can have a proximal bevelrepresenting a working channel and a distal bevel representing anepidural access needle and, potentially, an endoscopy port or anadditional working channel.

Referring now to FIGS. 16-19 and 42-45, an additional method andapparatus for placement of a tissue abrasion apparatus for selectivesurgical removal or remodeling of tissue is described. In FIG. 16, thedouble lumen epidural needle apparatus is positioned for advancementinto the epidural space 42. FIGS. 17 and 18 show how the covered andblunt tip of the epidural needle 2, double lumen epidural needle 84, orthe blunt end of the epidural endoscope, may be advanced into theipsilateral or contralateral lateral recess 108, towards the neuralforamen 110, in a direction parallel to both the adjacent ligamentumflavum 10 and the dura 46. In the illustrated example of the apparatusand method labeled FIG. 17, a fiberoptic element 38 has been placedwithin epidural needle 2, providing both a means for fiberopticvisualization of the epidural space 42 and a means to blunt the needleand thereby protect the tip of the needle from damaging the dura 46 orneural or vascular structures. In FIG. 18, the endoscope has beenadvanced along ligamentum flavum 10 (visually yellow, otherwise known as“the yellow ligament”) to the lateral recess 108. “Safe zone” 44designates the area in which a medical practitioner may resect, ablate,or otherwise modify tissue safely, directly visualizing the are oftissue modification through the fiberoptic element. The safe zone 44 isthe area posterior to the apparatus in the epidural space, where dura isknown to be on the other side of the apparatus, and is therefore a safezone for tissue alteration without damaging dura or central nervoussystem structures, particularly when using fiberoptic visualizationthrough the distal lumen. The second lumen of the two lumened needle 84or endoscope may be used as a working channel 50, or to dispense theabrasive element 14 and/or its protective sleeve 6, or the workingbarrier described in the primary patent referenced herein. After theneural foramen 110 has been cannulated with a non-sharp curved needle 16or catheter, and after the flexible, sharp, straight needle or wire 4(e.g., a guidewire) has been passed through the curved needle 16 untilits tip is advanced through the skin in the patient's back 70, theabrasion apparatus 14 and/or its sleeve or cover 6 are pulled throughthe neural foramen 110, as illustrated in FIGS. 43-45. The curved needle16 or tube may, for example, be fabricated from a spring steel, Nitinol,or other memory material that will allow it to be inserted through astraight needle, but to return to a fixed curve upon exiting thestraight epidural needle 2 or working channel 50. The curved needle 16optionally may be steerable. Preferably, the curved needle tip is notsharp, but is rounded or designed in other fashions less likely to cuttissue, in order to reduce a risk of neural or vascular damage.

In yet an additional embodiment of the invention (“portal over epiduralneedle” variation), an epidural portal 56 may be inserted into theepidural space 42 as a catheter over the epidural needle 2 (as in FIG.12), similar to the design for placement of standard intravenouscatheters used today. With such an approach, advancing the bluntedneedle (sharp tip covered) by several millimeters will also bring thedistal tip of the portal into the epidural space 42. Subsequently, theneedle may be withdrawn from the portal, which is held in place by thesurgeons other hand, leaving the epidural portal in the epidural space42 as a working channel or endoscope guide.

In one variation, the epidural needle 2, needle based endoscope,flexible or rigid endoscope, or portal 56 (for placement over anepidural needle 2) may have, preferably close to its distal tip, an(e.g., distal) anchor mechanism 40 and 48 (in its un-engaged position)that may be inflated or otherwise opened (e.g., in the epidural space42), to help prevent inadvertent removal of the device from the epiduralspace 42. It is expected that utilization of an anchor to, or within,the ligamentum flavum 10, will prevent the portal from being pulledinadvertently through the ligamentum flavum, and will enhance thereliability and safety of epidural access for minimally invasiveendoscopic surgery.

FIG. 14 illustrates additional methods of safely utilizing a bluntedepidural apparatus in conjunction with additional surgical tools. Safetool access may, for example, be facilitated with either a fixed workingchannel 50, as shown in FIG. 15, or by the creation of a rail 52 andslot 58 interface on the tool or epidural endoscope, cannula or“needlescope” 132, as shown in FIG. 14 b. The working channel 50 can beinsertable and removable and can be for attachment to the epiduralapparatus. The rail portion 52 of the epidural instrument can be forguiding the epidural tools along the blunted epidural apparatus into theepidural space. The slot portion 58 of the epidural instrument or portalcan be for guiding the epidural tool or working channel into theepidural space. Note the rail 52 and slot 58 may be reversed, with therail 52 on the sleeve or scope and the slot 58 on the tool or workingchannel.

FIG. 14 a shows a tool 54 (illustratively a grasper) fitted with a rail52 that mates with a slot 58 of epidural endoscope 132, so that it maybe inserted directly into the epidural space 42 and then advanced untilit is placed in the “safe zone” 44 (e.g., for tissue resection ormodification, on an opposite side of the epidural tissue), without theneed for a working channel along endoscope/needle 132. The part of theepidural tool that is expected to be in direct contact with theimpinging spinal tissues 124 that the surgeon intends to modify providesan ideal location for neural stimulator lead placement 130. In theexample illustrated in FIG. 14 a, an insulated tool shaft is combinedwith a conductive surface 130 on the tip of the grasping tool 54, to beused for neural stimulation. (note: the use of neural stimulation withsensorimotor monitoring, for neural localization, in conjunction withthe current invention, will be discussed later in this document)

In one variation, the epidural needle 2 is curved towards its distalend, e.g into a hockey stick shape. In a curved configuration, the lumenexits the bevel, distal to, and on the concave side of the bend in theneedle's distal shaft. With such a configuration, a “safe zone” 44 iscreated by inserting the needle so that the side opposite the bevel(convex side of the bend) is in direct contact with the dura, and thelumen, on the concave side of the bend, faces the ligamentum flavum.This configuration provides a “safe zone” 44, where tools, or a workingchannel 50, may be reliably placed on the needle side opposite the dura46.

In FIG. 14 b, a removable working channel 50 is disposed along epiduralneedle/endoscope 132, e.g., is integrally formed with the endoscope oris positioned via a rail 52 and slot 58 mating with the endoscope 132.FIG. 14 b illustrates an epidural “needlescope” 132 or endoscope cannulawith the working channel 50 in place, with its tool-presenting endadjacent to the “safe zone”.

Referring now to FIGS. 16-19, an additional method and apparatus forselective surgical removal of tissue is described. In FIG. 15, a doublebarrel epidural needle 164 is illustrated, comprising a working channel50 adjacent to the epidural needle 2. In FIG. 16, the double lumenepidural needle apparatus is positioned for advancement into theepidural space 42 (e.g., a safe triangle, an area at the most posterioraspect of the epidural space 42, where epidural needle 2 tip insertionis most consistently safely performed). In FIG. 17, a catheter basedfiberoptic element 38 has been placed within epidural needle 2,providing both a means for fiberoptic visualization of the epiduralspace 42 and a means to blunt the needle and thereby protect the tip ofthe needle from damaging the dura 46 or neural or vascular structures.In FIG. 18, the endoscope has been advanced along the ligamentum flavum10 to the lateral recess 136. “Safe zone” 44 designates the area inwhich a medical practitioner may resect, ablate, or otherwise modifytissue safely, under direct visualization. The second barrel or lumen ofthe double barreled needle 164 or endoscope may be used as a workingchannel 50, or to dispense a tissue modification barrier or workingbarrier or backstop 134.

In addition to the insertion of tools through the epidural needle 2, orthrough an adjacent working channel 50, the same channels may beutilized to insert a barrier 134, or “working backstop” 134 (FIGS. 19,20 b, 21 b, 22, 23, 24), into the spine. In a further variation of thepresent invention, a flexible, flat, thin mechanical barrier (“workingbackstop”) 134 is placed between the tissue to be resected and adjacentvulnerable neural or vascular structures that are desired to be leftintact and uninjured. The barrier provides protection for the dura 46,nerve root 62, dorsal root ganglia, and/or vasculature, by providinginsulation and/or preventing direct contact between the tools and thesevulnerable structures during tissue manipulation, resection, abrasion,or remodeling. The protective barrier may be placed between the needlebased or endoscopically delivered tools and the dura 46 in the centralspinal canal; in the lateral recess 136; or between the tools and theneural and neurovascular structures within the neural foramen 110. Thebarrier 134 may be placed through the neural foramen 110 anterior to thefacet joint 77, either anterior to the ligamentum flavum 10 (epiduralspace 42) or within or posterior to the ligamentum flavum 10 (posteriorto the epidural space 42). Tools that may be used in conjunction withthis barrier include, but are not limited to, cautery devices (monopolaror bipolar), lasers (erbium, etc.), rasps, ronguers, graspers, burrs,sanders, drills, shavers, or probes.

The barrier or backstop 134 may be placed percutaneously via a needle 2,endoscope 132, or double barreled needle 164. In addition to epiduralendoscopy, image guidance may be combined with the use of straight,curved, or steerable guidewires for the proper placement of the barrieror backstop 134. In an open surgical variation, the barrier or backstopdevice 134 may be placed through the surgical incision.

The barrier 134 may be synthesized from one of several possiblematerials, for example, it may be partially fabricated from a springsteel, Nitinol, polymers, or other memory material that will allow athin, flat barrier to be reconfigured into a more condensedconfiguration for passage through a straight needle [23 d], after whichit returns to its desired shape [23 c] upon exiting the needle 2. Thebarrier 134, optionally, may be steerable.

As is illustrated in FIG. 24, correct anatomic placement of the backstopdevice 134 may be validated via monitored electrical neural stimulationthrough the barrier device 134. Electrical nerve stimulation functionmay be added to the apparatus via dual conductive elements, the firstconductive element 104 for neural stimulation and localization placed onthe working side (e.g., on the surface) of the backstop (or the toolused on the working side or the epidural endoscope tip), where tissueremodeling and resection will occur. The neural stimulation delivery box114 can be attached to the ground electrode 116. In the exampleillustrated in FIG. 23, the working nerve stimulator on the working sideof the barrier may be integrated with the rail 128, through which nervestimulation may be tested before sliding the tool or sleeve over therail for tissue modification. A conductive element (e.g., for neuralstimulation) may also be placed on the non-working side of the backstop130. To gain accuracy in neural localization, the stimulation leads onthe device are separated by insulation material within the backstopmaterial.

The patient may be kept awake and responsive throughout this procedure,with no neuraxial anesthetics and no systemic analgesia. In this manner,the medical practitioner may, through verbal questioning, elicitresponses from the patient in order to ensure that any severe pain thatwould accompany undue pressure on the nerve root 62 during placement ofthe tissue modification device and/or during tissue removal orremodeling is immediately recognized prior to nerve injury.Alternatively, for a deeply sedated patient, or one under generalanesthesia, nerve stimulation may be monitored via SSEPs or SEPs;visually (motor movement of extremities); via MEPs; and/or via EMG(motor stimulation). In one embodiment of the device, one might use acalibrated sensor, combined with computer analysis, to accuratelyquantify neural stimulation at different locations, in order to moreaccurately localize neural structures.

As is illustrated in FIG. 24, there should be no nerve root 62 or dorsalroot ganglion stimulation in the exact location where tissue alterationis intended to take place, when one sends appropriate small electricalcurrent through an insulated electrode that is located on the workingside of an insulated working barrier, prior to tissue modification toolplacement. Correct neural location, relative to the tissue modificationtools and barrier may further be ensured by the addition of focusedneural stimulation functionality to accompanying surgical instruments.For example, tools used for probing, tissue resection, tissuecauterization, thermal treatment, tissue lasering, tissue manipulation,tissue retraction, and tissue abrasion may contain conductive elementsfor neural localization 104. The nerve stimulation capabilities may beused to ensure that the neural elements are not in dangerous proximity,or they may be used to assist with more concise neural localization. Forinstance, a probe fitted with neural stimulation capabilities in its tipmay be used to identify neural structures, through monitoring of sensoryor motor stimulation. However, electrical stimulation on the non-workingsurface of the working barrier, which is in direct or indirect contactwith neural structures, should result in motor and/or sensory actionpotentials, which may be monitored as described above, thereby providinga positive control and assurance of proper barrier placement. For addedsafety, a surgical device may be designed to automatically stimulatebefore or during resection, and may even be designed to automaticallyblock resection when nerve stimulation has been sensed.

In a preferred variation, impinging spinal tissue is removed usingtissue abrasion apparatus and method. Variations of the apparatus andmethod may be utilized during an open surgical procedure(s); during anendoscopic surgical procedure(s); or via a percutaneous (needledelivered) surgical approach. Use of a needle-based posteriorinterlaminar or interspinous approach, a posterior-lateralneuroforaminal approach or a minimally-invasive surgical approach forplacement of the neuroforaminal abrasive tissue removal device avoidsunnecessary tissue resection and minimizes tissue injury. In addition,further embodiments of the device include nerve stimulation andmonitoring capabilities, which, when added to a spinal tissue alterationdevice, may enable the surgeon to more safely perform the procedure.

FIG. 25 shows the needle tip anterior to the ligamentum flavum 10, butstill posterior to the dura 46 in the posterior epidural space 42. FIG.26 illustrates a preferred method of cannulating the neural foramina,where a blunt, curved needle composed of memory material 16 is passedthrough the straight epidural needle 2 (alternatively, a stiff epiduralcatheter 24, or steerable guidewire may be inserted through the needlefor this step). The curved needle 16 is flexible enough to be passedthrough the straight epidural needle 2, but is made of a memory materialthat returns it to its curved configuration upon when it is passed intotissue. The second needle 18 (alternatively, a steerable, stiffcatheter, needle or guidewire), is advanced through the epidural space42, possibly passing through a portion of the ligamentum flavum 10,towards and then through the ipsilateral or contralateral neural foramen110. The surgeon may use any combination of tactile feel, imageguidance, direct visualization, and/or fiberoptic visualization toensure that the curved element 16 is driven through the neural foramen110, anterior to the facet (zygapophysial) joint complex 12, butposterior to the nerve root 62 or ganglion. Once the curved element isin position through the neural foramen 110, the surgeon subsequentlypasses a smaller gauge straight and sharp flexible wire 4 (or needle),as in FIG. 27 through the lumen of the larger curved needle that is inposition through the neural foramen 110, until it exits into the tissuelateral to the neural foramen 110 (FIG. 27). This straight wire 4 orstraight needle exits the curved element with its tip facing in aposterior or posterior-lateral direction. It is advanced further in thisdirection, passing to, and then through the skin of the patient's back70, as in FIG. 27.

Studies and tests may be performed to ensure that the transforaminallyplaced apparatus has been properly positioned between the nerve root 62or ganglia and the facet joint complex 12. For example, imaging of theabrasion element and spinal anatomy (fluoroscopic or other imagingmodalities); monitored neural stimulation through the apparatus; ordirect (endoscopic or open) visualization may be utilized.

After proper placement has been confirmed, the curved element 16 thatwas used to initially cannulate the neural foramen 110 is removed, bypulling it back out of the hub of the epidural needle 2, leaving thetransforaminal wire 4 in place, as illustrated in FIG. 28. Next theepidural needle 2 may also be removed, if desired, again leaving thewire 4 in its position, through the neural foramen 110. As shown, bothends of the element remain external to the patient, having exited theskin (percutaneous procedure) or exited the tissue through the surgicalwound (open procedure).

With the wire in position through the neural foramina, there aremultiple possible methods for replacing the wire with the abrasionapparatus. One method is illustrated in FIGS. 43-45, where the wire 4 isused to pull into position the abrasion element 14; the abrasion elementsleeve or cover 6; or the abrasion element 14 and cover 6 together, asis described in greater detail below. Alternatively, as shown in FIGS.29 and 30, separate protective sleeves or covers 6 may be passed overboth the proximal and distal ends of the transforaminal wire 4. Eachsleeve or cover may be advanced to the neural foramen 110. Next, theneuroforaminally placed wire 4 is connected distally, or proximally, tothe abrasive element 14, with an abrasive surface on one side. Theabrasive element 14, connected by one end to the transforaminal wire 4,is pulled through the neural foramen 110, and through the protectivesheaths or covers 6, as in FIGS. 31 and 32, until the abrasive element14 has completely replaced the initially placed wire 4 (or needle).Passage of a tissue dilator over the transforaminal wire 4 or needle,may be helpful, either before or after placement of the sleeve.Protective sleeve(s) 6 illustratively are disposed over both ends of thetransforaminal wire 4, in order to protect non-surgical tissues from theabrasive or cutting portion of the device, when it is pulled into place.Alternatively, a protective abrasive element sleeve 98, which may beexpandable, as illustrated in FIG. 83, may be attached to the end of thewire and pulled through the neural foramina, thereby replacing theinitial transforaminally placed element. The abrasive element sleeve 98covers the abrasive element in tissue and is a conduit for insertion andexchange of abrasive elements.

In an alternative preferred embodiment, the abrasive element 14 ispositioned within the protective sleeve cover 6, before or afterplacement of the abrasive element in position through the neuralforamina. Please note that the terms “protective sleeve” and “protectivecover” are used interchangeably in these descriptions of severalexamples of the apparatus and methods for protecting vulnerable tissuefrom the abrasion apparatus. Embodiments of the protective methods andapparatus are illustrated in FIGS. 82-85. With the abrasive element 14already inside the protective apparatus 6 or 96, with or without anopening over the abrasive surface where tissue abrasion is to beperformed the protective covering, with the abrasive apparatus alreadyinserted within it, may be connected to one end of the needle orguidewire that remains in place through the neural foramen 110. In thispreferred method, the combined protective sleeve and 6 the abrasiveelement 14 are then pulled simultaneously through the neural foramen110, by pulling from the opposite end of the preliminarily placedneuroforaminal element, while it is removed. A conductive element 90 forneural stimulation can be on the working side of the apparatus.

Once the abrasion apparatus has been properly positioned through theneural foramina, with its protective cover in place, it is ready to betested to ensure it has been properly located. The apparatus maysubsequently be utilized for tissue abrasion, tissue removal, and tissueremodeling, as will be described in detail below. Before describingtissue modification in further detail, however, we will describealternative approaches for placement of the abrasion device intoposition through the neural foramina.

Referring now to FIGS. 33-36, a variation of the method and apparatus ofFIGS. 25-32 is described comprising an alternative approach forplacement of the tissue modification device, wherein the apparatus 14 isplaced from the lateral side of the neural foramen 110. As seen in FIG.33, a steerable or needle wire 18 is placed through the neural foramina110 from the lateral towards the medial side of the foramen 110. Thislateral to medial neuroforaminal approach may begin with a curved, bluntwire through a straight needle (as described in the previous technique),or using a curved needle technique, a steerable guidewire technique, aneedle-through-a-needle technique, or common variations thereof. FIG. 36illustrates that the protective sleeve 6 or cover can have a neuralbarrier portion 8 for the abrasion element. While a loss of resistancetechnique is not as helpful with this transforaminal approach to theepidural space 42, as it was in the previously described posteriorapproach to the epidural space 42, the method is, in many other aspects,otherwise similar to the method illustrated in FIGS. 25-32.

With reference to FIGS. 37 a-e, another variation of the method andapparatus of FIGS. 25-32 is described. In FIG. 37 a, the apparatus 20 isplaced from an interlaminar; a translaminar, interspinous; or atransforaminal insertion, illustratively via a paramedian, ipsilateralapproach. A lateral to medial transforaminal approach with the same typeof apparatus may alternatively be used. The blunt or rounded distal tipof apparatus 20 optionally may be somewhat sharper, to facilitateplacement. The apparatus 20 may be preceded by a guidewire, a dilator,or a needle iritroducer (possibly with or followed by an expandablesheath). This variation of the apparatus and method, as seen in FIG. 37b, contains a rigid, curved wire or needle 22, which may be steerable,which is driven from the tip of the apparatus 20, laterally through theneural foramen 110 and then posteriorly, around the facet joint complex12 and back towards apparatus 20, where the needle may be received onceagain by the apparatus. Arrow 26 in FIG. 37 d illustrates the directionof movement of the abrasive element. FIG. 38 provides a cross sectionthrough apparatus 20 that illustrates an exemplary geometry for theapparatus comprising a feature that facilitates receiving of the distalend of the needle or rigid guidewire back within the apparatus.Alternative geometries will be apparent. Once received back withinapparatus 20, the wire 22 completely encircles the facet joint 12, as inFIG. 37 c, d. In FIGS. 37 d, 38, and 39, guidewire 22 has been replacedby tissue abrasion device 32, e.g., a belt, strap or ribbon, preferablywithin a protective sheath or cover, with the abrasive surface of thedevice in contact with the anterior-medial facet complex. Apparatus 20is pulled back, bringing the working surface (exposed abrasive portion)of the instrument into firm contact with operator controlled pressureagainst the surface from which tissue removal will occur. Neuroforaminalenlargement begins with the movement of the abrasive surface 30 againstthe anterior and medial portion of the facet complex 12, in the lateralrecess and neural foramen 110. The abrasive surface 30 can be of anabrasive element in an electromechanical abrasion device.

With reference to FIG. 38, an enlarged view of the mechanical portion ofapparatus 20 is described. An abrasive surface 30 is disposed along theinside side of tissue abrasion element. The abrasion device may beactuated, e.g., via rotation of a gear 106 within the apparatus 20. Thegear or knob 106 engages with the abrasive element, and is turned toprovide movement of the abrasive element within the apparatus. Debrismay be captured within apparatus 20, and stored in the shaft and/orhandle 68, or removed continuously during the procedure. The debris canbe sent in the direction of arrow 180 for removal or storage.

Referring now to FIG. 39, a variation of the apparatus of FIG. 38 isdescribed comprising an additional protective cover 32 that covers oneor more sides of the abrasive elements 14 of the device 20 in allregions except for the area covering the tissue where abrasion is totake place. This cover may contain a conductive element in order toenable nerve stimulation 130 and/or to facilitate neural localization104. Nerve stimulation capabilities may be present on the internalabrasive surface 30 of device abrasive element 14, and/or on theexternal side (non-tissue abrading) of the device, as an added safetymeasure. For example, the user may send an electric impulse through aconductive element within the back-side (external surface) of thedevice, expecting to achieve neural stimulation when the device is inplace through the neural foramina, while neural stimulation should notbe achievable with a similar electrical impulse conducted across aportion of the abrasive side of the device. In this manner, informationfrom monitoring the nerve stimulation may ensure proper placement of theabrasion device and reduce a risk of inadvertent neural or perineuralvascular abrasion.

In FIG. 40, straight wire or needle 4 is driven through curved needle 16disposed in working channel 50 of double barrel epidural needle 164.This straight wire or needle is advanced until it has penetrated throughthe skin and out of the patient's body. The straight wire preferably hasa sharp tip. In FIG. 41, the curved needle 16 has been withdrawn fromworking channel 50, leaving straight wire or needle 4 in place. Then, asseen in FIG. 42, the epidural needle 2 and working channel may bewithdrawn from the patient, or, in an alternative embodiment (FIG. 14b), when using a detachable working channel 50, the working channelalone may be withdrawn from the patient, leaving straight wire 4 inplace. In FIG. 43, straight wire 4 has been hooked to abrasion device 14and/or the abrasion device's protective sleeve 6. In FIG. 44, theabrasion device 14 and/or the device's protective sleeve are pulled intoposition by wire 4 as the wire is removed. In FIG. 45, wire 4 has beencompletely removed, and the abrasion device 14 and its protective sleeve6 are properly positioned for tissue resection, anterior to the facet 12and ligamentum flavum 10.

In an open surgical variation, the abrasive element 14 and its cover 6may be placed through the surgical incision, from a interlaminar,translaminar, or neuroforaminal approach. Visualization and placementmay be aided via partial or complete laminectomy, facetectomy, orligamentectomy. Methods for threading the neural foramina include, butare not limited to the use of a wire, blunt needle, probe, endoscope, orsuture. After spinal neuroforaminal placement, the abrasion device 14 isused to selectively remove tissues that impinge on the neurovascularstructures within the lateral recess 108 and neural foramen 110, on theanterior side of the facet joint 12. In an open approach, as with apercutaneous approach, the device may be inserted through a needle,optionally under image guidance or with the aid of an epiduralendoscope. Once placed through the neural foramina 110 of the spine,around the anterior border of the facet joint 12, and anterior to theligamentum flavum 10, the medical practitioner may enlarge the lateralrecess and neural foramina via frictional abrasion, i.e., by sliding theabrasive surface across the tissue to be resected (e.g., far lateralligamentum flavum 10, anterior and medial facet, osteophytes). Theabrasion device alternatively or additionally may be placed through theneural foramen 110 anterior to the facet joint 12, but through orposterior to the ligamentum flavum 10. The medical practitioner controlsthe force and speed of the abrasive surface against the tissue to beremoved, while optional protective covers, tubes or sleeves 6 help limitthe area exposed to the abrasive element for treatment.

Referring now to FIGS. 46-61, a variation of the method and apparatus ofFIGS. 40-45 is described, comprising another preferred approach forplacement of the abrasion device. This series begins with FIG. 46, inwhich a double lumen, blunt tipped, epidural device 84, has already beenadvanced to the lateral recess 108, using a technique similar to FIG.18. Next, FIG. 47 shows a curved flexible needle 16, preferably with anatraumatic tip, that has been advanced, via the working channel 50 (FIG.15), through the neural foramina 110. FIG. 48 illustrates threading ofthe straight, flexible, sharp tipped wire 4 a through the curved needle16, and advanced posteriorly until it exits the skin of the back 70. InFIG. 49, the curved needle has been withdrawn, leaving the straight wire4 a in place. In FIG. 50, the double lumen epidural apparatus 84 isslightly withdrawn, from the patient, so that the working channel 50 isdirected towards the medial side of the facet complex 12. FIG. 51 showsthe curved needle 16 advanced through the working channel again,adjacent to the first wire 4 a, this time advancing the same or adifferent curved, flexible needle 16, towards the opposite side of thefacet complex 12. FIG. 52 shows where a second straight flexible wire 4b is advanced through the second placement of a curved needle 16, thistime on the medial side of the facet joint. The second sharp, flexible,straight wire 4 b is threaded through this second curved needle, andsubsequently advanced posteriorly, until the sharp tip of the wire 4 bexits the skin. FIG. 53 next shows both the curved needles and thedouble lumen apparatus removed, leaving the wires 4 a and 4 b in place.FIG. 54 shows that both wires have been attached to the two ends of theabrasive element and/or the cover 32 of the abrasive element.Alternatively, the two wires 4 a and 4 b may be opposite ends of thesame continuous wire, with the cover 32 for the abrasive element alreadyplaced over the mid-portion of the wire 4. Alternatively, the abrasiveelement 14 may already have been placed inside said cover 32, andattached at each end to the wires 4 a and 4 b. FIGS. 55 and 56 show thetwo wires 4 a and 4 b pulled and bringing the abrasive element cover,possibly with the abrasive element 14 already placed inside said cover32, into position through the neural foramina. FIG. 57 illustrates thestep that follows placement of the abrasion element cover alone. In FIG.57, with the wire in place inside the abrasion element cover 6, theabrasive element 14 is now seen to have been attached to the end of thewire. Subsequently, the cover 32 is held open at each end by a graspingdevice, which also holds the cover under tension against the tissue tobe abraded. With the cover anchored thus, the abrasive element is pulledinto place by the wire, replacing the wire, as has occurred for FIGS. 58and 59. With the abrasive element in position and the abrasive elementcover tightly held open and against the tissue to be abraded, theabrasion element 14 may be pulled back and forth, under tension, againstthe tissue to be abraded, as in FIG. 59. Alternatively, the abrasiveelement may be pulled in a single direction across the tissue to beabraded. FIG. 60 illustrates the cover following removal of the abrasiveelement. Said cover may remain in placed as a compression bandage 168,under tension against the freshly abraded surface, in order to promotehemostasis, promote tissue remodeling, and trap debris post operatively.The compression bandage 168 can be a percutaneous retention andcompression dressing or tissue remodeling strap, or a retention strap orbelt.

A nerve stimulator may be incorporated into the abrasive surface of theabrasive element, and/or incorporated into the protective cover 88 orsheath for the abrasive element, in order to verify correct placementand enhance safety by allowing the medical practitioner to ensure thatneural tissue is not subject to inadvertent abrasion. FIG. 61illustrates a neural stimulation apparatus. FIG. 61 also illustrates anabrasion element 14, disposed inside of a sheath or cover 6, and held inplace by tension retaining elements 112 (shown in FIG. 60). The skinanchor 112 for the abrasive element cover or sheath can hold the coverunder tension, allowing the abrasive element to be moved freely within.The stimulation apparatus 114 (e.g., the neural stimulation deliverybox) delivers a small electrical current through the working surfaceand/or the non-working surface (backside) of either the tools used inthe epidural space 42, the abrasive element, and/or the protective coverof the abrasive element. Preferably, one electrode, or wire 120 to theelectrode, would be connected to each side (abrasive and non-abrasive)of the entire device and sheath complex, along the full distance wheretissue abrasion is planned to occur, in the lateral recess, centralcanal, or neural foramen 110. Neural stimulation may be monitored viaverbal response to stimulation in an awake or lightly sedated patient,or SSEP, MEP, EMG, or motor evoked muscular movement in an asleep orsedated patient. One possible mechanism for avoiding inadvertent neuraldamage may be to ensure that there is no neural stimulation whenstimulating the working surface of the device. A positive control shouldbe obtainable in the lateral recess and neural foramen 110, whenstimulating the non working surface (back side) of the device or,preferably, the backside of the device cover or sheath 172 (e.g., firstportion of locking mechanism).

After the abrasion element, and possibly its protective sheath or cover[3, 49, 50], have been placed through the neural foramina 110 theabrasive surface is brought into firm contact with the tissue to beabraded by pulling tension simultaneously on each end of the abrasionelement. When both ends of the abrasive element 14 are pulledsimultaneously, the abrasive surface of the device is brought undertension and into firm contact with the impinging spinal tissue on theanterior and medial sides of the facet joint complex 12. Subsequently,one end of the abrasive element is pulled more forcefully than theother, sliding the abrasive surface is across the target tissue. Whenone end of the abrasive element is pulled with more force than theother, the ribbon moves in the direction of the stronger pull, while thelesser pull on the opposite end maintains force and creates frictionwith movement between the abrasive surface and the tissue to beresected. When the optional protective cover 6 or sheath is provided,both of its ends of the are, in one variation, pulled under traction andanchored in place, such that the abrasive element 14 may be pulled ineither or both directions through the cover 6 or sheath withoutsignificant friction against and/or without causing trauma to adjacenttissues.

Alternatively, the abrasive element 14 may be pulled in a singledirection across the tissue. The abrasive belt, strap or ribbon may be asingle length, pulled alternately in each direction, or it may bedispensed from a spool, as in FIG. 62 a, or from a reel to reelconfiguration, as in FIG. 62 b, and pulled in both directions or pulledin a single direction, across the tissue to be abraded. An alternativevariation of the apparatus and method utilize an electromechanical, beltdriven abrasive tool, an example of which was described previously inFIGS. 38 and 39.

In one variation of the invention, a tissue retention or compressiondressing (FIGS. 60, 70, 72) method and apparatus are utilizedimmediately following the tissue removal, ablation and remodelingprocedures described previously. For example, following neuroforaminaland lateral recess enlargement, it may be advantageous to leave, as asurgical dressing, a thin flat element 150 pulled tightly against theresected, abraded, or remodeled tissue surface (e.g., around the facetcomplex 12). The neuroforaminal compression element can be placed aroundthe facet complex. It is expected that a compression dressing of thisnature will enhance hemostasis, promote healing and promote subsequenttissue remodeling with the neural foramen 110 widely open. Furthermore,the surgical dressing 150 would provide a barrier to trap tissue debrisaway from neural or neurovascular structures, while providing anoptional technique for delivering medication, possibly as a depot, tothe operative site. The dressing 150 would also present a smooth surfacetowards the nerve root 62 in the immediate post-operative period.

As in FIG. 60, this neuroforaminal compression dressing may bepercutaneously held tightly in place against the resected, abraded, orotherwise remodeled surface (e.g., zygapophysial (facet) joint) 77. Incertain embodiments, the compression dressing may be eitherpercutaneously removable (as shown in FIGS. 60 and 70), either bypulling the dressing through the neural foramen 110, or by the inclusionof a biodegradable central component of the dressing, such that the twoends may be removed, with the dressing separating at its biodegradableportion in the middle. Other variations such a compression dressinginclude a totally implanted and completely biodegradable dressing, asillustrated in FIG. 72 a or b. FIG. 72 a also illustrates the transverseprocesses.

FIGS. 46-56 and 60, and FIGS. 63-70 illustrate midline or paramedianapproaches to percutaneous placement of a neuroforaminal compressiondevice (e.g., percutaneous retention compression dressing or tissueremodeling strap) 155 that is wrapped around the facet complex 12 andretracts the posterior aspect of the neural foramina, effectivelydilating the space available for the neural and vascular structures.FIGS. 67 a and b illustrate the first steps in a posterior lateralneuroforaminal approach to placement of a compression element(subsequent steps would share similarities with the approach illustratedin FIGS. 46-56 and 60). A grasper, loop or hook 146 can be for grabbingan end of the guidewire.

An additional embodiment of the method and apparatus may combine boththe working backstop 134 and the compression element 150, 155, asillustrated in FIGS. 73 and 74. In these illustrations, the compressionelement 150, 155 serves to keep the working barrier 134 in properposition. Subsequently, image guidance may be used to guide tools usedin open or percutaneous procedural approaches to neuroforaminal andlateral recess enlargement. The example in FIG. 74 illustrates an imageguided drill 176 removing a portion of the impinging facet complex 12.With the barrier in place, possibly further aided by neuralstimulation/localization capabilities, selective and safe tissue removalmay be more readily performed.

FIGS. 75-78 illustrate some of the compression element embodiments 150,155. FIG. 76 also contains an area (e.g., a drug depot in a retentionstrap or compression dressing) 162 for storage of medications fordelivery to the tissue retracted by the compression element 150, 155.The compression element can have a locking mechanism that can have afirst portion 172 that can insert through a second portion. Thecompression element can have a locking mechanism that can have a secondportion 174 that can receive a first portion 172.

FIGS. 79 and 80 demonstrate additional methods and apparatus forenlargement of the central spinal canal and lateral recess, byretracting the posterior spinal anatomy, in particular the ligamentumflavum 10 (FIGS. 79 and 80 illustrate translaminar ligamentum 10retraction), in a further posterior direction, away from the dura 46,cauda equina 140, nerve roots 62, and dorsal root ganglia. Such a devicewould both serve both to retract the spinal tissue posteriorly, and toprevent the posterior elements, particularly the ligamentum flavum 10,from buckling anteriorly 138 into the spinal canal or lateral recess.FIG. 79 illustrates an apparatus with an anchor 126 anterior to orwithin the ligamentum flavum 10, a second (e.g., laminar) anchor 166posterior to the lamina 122 (e.g., for posterior retention) and amechanism for maintaining tension in order to retract the tissuesposteriorly, towards the lamina 122. FIG. 80 illustrates a rivet typedevice that is placed through a hole that has been drilled through thelamina 122. Such a rivet has an anchor 126 placed anterior to theligamentum flavum 10, which is retracted posteriorly in order to enlargethe central spinal canal and/or lateral recess. Spinal endoscopy may beused as a tool to place a ligamentum flavum 10 retraction system, or inorder to confirm that correct placement and efficacy has been achieved.

Most of the safety issues related to the methods and apparatus describedherein are similar to those associated with any surgical procedure,e.g., infection and/or bleeding. Some safety issues are more specific tosurgery in and around the spine or spinal cord, and are therefore givenspecial consideration below. These generally relate to spinal nerveinjury. Morbidity could result from instruments inadvertently passedthrough the dura mater 46, and creating a cerebrospinal fluid leakand/or damaging the cauda equina 140 (below T12-L1) or spinal cord(above T12-L1) when entering the epidural space 42. Potentiallytraumatized structures further include nerve roots 62, adjacentvasculature, or dorsal root ganglia.

FIG. 81 are sagittal midline cryosections of the lumbar spine, providedcourtesy of Wolfgang Rauchning, Md., that demonstrate the ligamentumflavum 10 protruding (“buckling”) anteriorly, a potential mechanism forcentral or lateral recess neural or neurovascular impingement. Theligamentum flavum 10 is a potential target for abrasive tissue resectionusing the herein described methods and apparatus.

FIGS. 82, 83, 84, 85, 87 illustrate preferred embodiments of theprotective cover or sheath for the abrasion element, in which theabrasive surface is covered 98 and the backside of the abrasive elementmay also be shielded 48, to prevent tissue damage in areas where tissueabrasion is not intended. The abrasive element's protective cover 6 isideally shaped to provide optimal protection of vulnerable tissues, atthe same time maintaining both a very small profile, for easy threadingof the stenotic neural foramen 110; and atraumatic edges (e.g. rounded),in order to prevent cutting of or trauma to neural, vascular or othertissue during placement, use or removal of the device. For example, incertain preferred embodiments, the abrasion device may be tubular (FIG.82), with an opening over the tissue to be abraded; or may be flat(FIGS. 83, 84, 85, 87) with atraumatic railings or tracks thatfacilitate passage of the abrasion element, abrasion surface cover, orother instruments. Side channels 82 (e.g., the edge of the backing forthe abrasive element), through which the edges of the abrasion elementmay be maintained or held but are able to slide freely may be of anatraumatic shape. Said side channels may also hold the protective cover94 for the abrasive side of the abrasion element 14. Note that neuralstimulation and localization may be performed through a conductiveelement 86 in the back cover, the front cover (e.g., a strap tensionelement 170), or in the abrasive side of the abrasive element itself 14.Both free ends of the device, as well as the ends of the optionalprotective sheath or cover, are positioned external to the patient formanipulation by a medical practitioner.

FIG. 84 show a similar protective cover and abrasive elementconfiguration to that described in FIG. 83, this time with neuralstimulation element 92 only illustrated in the non-abrasive (e.g.,non-working) side of the apparatus (e.g., protective cover). Inaddition, FIGS. 84 e and 84 f show that the abrasive element 14 has beenreplaced by an alternative element for drug deposition 88 (e.g., a drugdepot strip for insertion into the compression strap, working backstopor barrier device; a retention strap or belt, or a compression bridge),and/or to serve as part of the compression dressing, when the elementsare left under tension against the abraded surface, after the operativeprocedure.

FIG. 85 illustrate an additional similar embodiment of the abrasiveelement 14 with protective covers 94, 96: the removable cover 94 for theabrasive (i.e., working) side of the of the abrasive element, and theprotective working barrier 96 (i.e., the working backstop) for theabrasive element. This time, no neural stimulation elements areillustrated.

Referring now to FIGS. 86 and 87, cross sections through the abrasiveapparatus are illustrated. The abrasive element 14 is seen, housedwithin the protective covers. As shown, the abrasion element may, forexample, be structured as a thin belt or ribbon, with an abrasive 102and/or cutting surface 100 on one of its sides. The cutting surface 100can be an abrasive surface of the apparatus with a miniature bladedesign. The abrasive surface 102 can be an abrasive surface of theapparatus with a sandpaper design. The abrasive element 7 may exist in avariety of shapes, ranging from flat to curved; from narrow to wide; andfrom a solid to perforated. The abrasive surface of the abrasive elementmay, in one variation, contain deep grooves 118 or perforations for thetransport, collection and removal of (tissue) debris away from theoperative site. Alternatively, the pattern of abrasive may be designedto control the direction and speed of movement of the surface across thetissue to be abraded (e.g. deep grooves 118, at a diagonal to the edgeof the straps, may be used to facilitate lateral movement of theabrasive element). The width and shape of the abrasive elements may alsobe varied, in further effort to control the area of tissue to beresected. Finally, in one preferred variation, the surgeon would beginwith a coarser grade of abrasive material, in order to gain moreaggressive tissue removal. Sequential use of less and less aggressivesurfaces would serve to smooth the abraded tissue surface, with the aimof creating an atraumatic surface for contact with neurovascularstructures.

Placement of a tissue abrasion device 86 through protective sleeve(s)and 48 into position for selective tissue removal, brings the abrasivesurface into contact with the tissue to be removed. A medicalpractitioner may remove tissue in contact with abrasive surface (FIGS.87 a, b, c) by applying a reciprocating or unidirectional motion to theends of device 86 exterior to the patient. In one variation, a spool orreel to reel configuration may be designed that begins with a coarsegrade of abrasive material, and progresses towards less abrasivematerials as the spool or reel unwinds.

In one variation, the device includes a compression dressing asillustrated in the percutaneous embodiment described above in FIGS. 60and 61. Following neuroforaminal and lateral recess enlargement, it maybe advantageous to leave, as a surgical dressing, a belt or ribbonpulled tightly against the abraded tissue surface. It is expected that acompression dressing will enhance hemostasis, promote healing andpromote subsequent tissue remodeling with the neural foramen 110 widelyopen. Furthermore, the surgical dressing would provide a barrier to traptissue debris away from neural or neurovascular structures, whileproviding an optional technique for delivering medication, possibly as adepot, to the operative site. The dressing would also present a smoothsurface towards the nerve root 62 in the immediate post-operativeperiod.

The neuroforaminal compression dressing may, in one preferredembodiment, comprise the optional protective sheath, percutaneously heldtightly in place against the abraded surface, after the abrasiveapparatus has been removed from its lumen, for a period of time.Alternatively or additionally, a separate percutaneously removablecompression dressing may be placed following tissue abrasion. Theabrasive material may be followed by a length of compression dressingmaterial on the same reel or spool, or a subsequent reel or spool.Alternatively, a compression dressing may be delivered through theneural foramen 110 as a separate element. The compression element mayalso be used to deliver medications or other bioactive components (e.g.steroid, biodegradable adhesion barriers, etc.), to the surgical site.The compression dressing material may be, in one variation, partially orcompletely biodegradable. An entirely biodegradable compression dressingmay be placed tightly against the abraded surface, and left completelyimplanted following the procedure.

Whether placing the apparatus with an epidural needle 2; through theworking channel of an epidural needle e.g. 50; with an epiduralendoscope; or during an open surgical procedure; image guidance may beused to facilitate safe and accurate placement. If the epidural needle 2has been replaced by, or converted to, an endoscope, directvisualization of the epidural space 42 may be accomplished. In thiscase, as illustrated in FIGS. 88-99, the clear tip of the fiberopticscope will facilitate visualization through the fat present in theepidural space 42. The fiberoptic cable may be rigid or flexible. Theendoscope fiberoptic cable tip may be straight or angled, with the flatsurface of its distal tip 66 perpendicular (0°, for straight aheadviewing) or at an angle (e.g. 30°, 45°, or 60°). The cannula or portal(e.g., an epidural endoscope) may be closed at its tip or end 76, as inFIGS. 88-99, covering and protecting the distal end of the fiberopticcable with a clear tip 74 which may be solid, fluid, or gas filled,potentially sized and shaped to expand the area of viewing within thefat filled epidural space 42. Additionally the endoscope or“needlescope” may contain an additional channel or space for infusion offluid into the epidural space 42, in order to facilitate visualization,to create a space for visualization, and/or to decrease bleeding byincreasing pressure, towards or above venous pressure, within theviewing area.

FIGS. 88 through 99 illustrate several embodiments of closed tip portalsfor epidural fiberoptic visualization. Some description of these portalsmay be found in the text above. Basically, the portals show severalpreferred variations of designs that enable visualization through thefat that exists in the epidural space 42. The clear tips of the portalsmay be solid and clear, or may contain air or clear liquid. The volumeof the tip creates a space for improved perspective duringvisualization.

Referring now to FIG. 88, a hockey stick shaped portal facilitatessteering of the portal by rotation of the device. Such a design may beused with a flexible, partially flexible, or rigid fiberoptic element64. Besides steering the portal tip, the fiberoptic element may berotated separately in order to direct visualization, when angled scopetips are used (e.g. 30°, 45°, 60°). Alternative embodiments, asillustrated in FIG. 92, may allow the flexible neck (i.e., tip) 72 ofthe instrument (e.g., the clear tipped epidural endoscope portal) to besteered. FIGS. 94-96, 98, and 99 illustrate means of delivering toolsalong with the epidural endoscopic portals. Finally, FIG. 97 show acouple of different shapes of the many possible variations that may behelpful in improving visualization and access to the central canal,lateral recesses, neural foramen 110 and posterior annulus of the spine.

Many of the safety issues related to the methods and apparatus describedherein are similar to those associated with any surgical procedure,e.g., infection and/or bleeding. Some safety issues are more specific tosurgery in and around the spine or spinal cord, and are therefore givenspecial consideration below. These generally relate to spinal neural andneurovascular injury. Central Nervous System injury could result frominstruments inadvertently traumatizing the dura mater 46 when enteringthe epidural space 42, injuring the nerve root(s) 62, the adjacentvasculature, or the dorsal root ganglion as the apparatus is advancedand utilized towards and through the neural foramen 110.

Several techniques may be used to reduce a risk of dural, neural orneurovascular injury, including potentially traumatizing structuresincluding nerve roots 62, adjacent vasculature, or dorsal root ganglia.For example, the tissue alteration (e.g., abrasion) devices may beplaced under direct visualization when utilizing an open surgicalapproach or technique. Likewise, image guidance may be provided duringplacement or to confirm correct placement. Candidate image guidancetechniques include fluoroscopy, fluoroscopy alone, fluoroscopy withadditional technology for triangulation and tracking of instruments(e.g. infrared, RF, etc.), MRI, CT, OCT, ultrasound, etc. Catheters orguidewires may include their own image guidance capabilities such ascatheter or guidewire-based image guidance, e.g., fiberopticvisualization, catheter-based ultrasound, catheter-based MRI, opticaltomography, etc. Alternatively or additionally, endoscopic visualizationmay be utilized (e.g. flexible fiberoptic endoscope as in Epiduroscope,or via rigid surgical endoscopes), during placement and/orpost-placement confirmation of correct placement.

In addition to epidural endoscopy, image guidance may be combined withthe use of straight, curved, or steerable guidewires for the properplacement of the neuroforaminal abrasive element. Placement may beachieved percutaneously or through a surgical incision. Such a devicemay be implanted as an adjunct to an open surgical procedure(s); as anadjunct to an endoscopic surgical procedure(s); or as a separate open,image-guided percutaneous or endoscopic surgical procedure. Percutaneousapproaches will enable the surgeon to perform the procedure under localanesthetic in awake or sedated patients, if desired. As discussed, nervestimulation and localization capabilities may be added to the device inorder to enable the surgeon to more safely perform the procedure in ananesthetized, but un-paralyzed patient.

It is expected that the apparatus and methods of the present inventionwill facilitate a minimally invasive approach to the selectiveelimination (e.g., alteration, ablation, removal) of pathological spinaltissue, thereby enabling symptomatic relief in patients suffering fromspinal stenosis. Spinal neural and neurovascular impingement causetremendous pain and disability, with symptoms that include back and legpain, weakness, and decreased sensation. Neural ischemia and injurycaused by compression and inflammation may result in a wide range ofsymptoms or degrees of nerve damage. Symptoms range in severity frommild to severe, and from intermittent to permanent. For example,neurogenic claudication, which is exacerbated by back extension (asoccurs when one stands erect and places the spine in extension), may bemild or severe. Symptoms of neurogenic claudication are usually improvedby changes in posture that lead to back flexion, such as sitting. Themost severe cases of spinal stenosis may lead to permanent neurologicaldamage, including the possibility of the development of cauda equinasyndrome.

Spine surgeons lack safe and effective techniques or tools to minimallyinvasively or percutaneously reduce neural and neurovascular impingementin the spine, while minimizing collateral tissue damage. It is expectedthat the apparatus and methods of the present invention may be utilizedfor lateral recess and neuroforaminal enlargement to provide adequatebone and soft tissue resection, while reducing unnecessary destructionof functional bone, ligament or muscle in order to gain access to thetissues to be resected or modified.

Because critical neural and neurovascular structures are in closeproximity to the areas where surgical manipulation, dissection,resection, ablation and remodeling would be therapeutically valuable inthe spine, safety at each step in the procedure is of criticalimportance in order to avoid disabling neurological damage to thepatient. For this reason, safety measures, such as working barriers andnerve localization via an integrated nerve stimulator, are described.

Although preferred illustrative embodiments of the present invention aredescribed hereinabove, it will be apparent to those skilled in the artthat various changes and modifications may be made thereto withoutdeparting from the invention. It is intended in the appended claims tocover all such changes and modifications that fall within the truespirit and scope of the invention.

1. A system for use in treating tissue, the system comprising: acannula; a barrier device comprising an elongate member having aflexible flat distal section, where the flexible flat distal section isconfigured to be advanced through the lumen of the cannula and afterexiting from the cannula can expand to form a shield having a crosssectional area greater than that of the lumen of the cannula; and atleast one electrode located on the barrier, the electrode adapted to becoupled to a neural locating device.
 2. The system of claim 1, furthercomprising a second electrode on the barrier device, where the secondelectrode is adapted to be coupled to the neural locating device.
 3. Thesystem of claim 1, further comprising a cannula electrode located on thecannula, where the cannula electrode is adapted to be coupled to theneural locating device.
 4. A surgical barrier device for use with anerve locating apparatus, the barrier device comprising: an elongatemember having a flexible flat distal section, where the flexible flatdistal section is configured to be collapsible to reduce in profile; atleast one electrode attached to the flat distal section; and a connectorfor electrically coupling the electrode to the nerve locating apparatus.5. The surgical barrier of claim 4, where the electrode is located on atleast a top or bottom surface of the flat distal section.
 6. Thesurgical barrier of claim 4, where the at least one electrode comprisesat least two electrodes, and where an electrode is located on a top andbottom surface of the flat distal section.
 7. The surgical barrier ofclaim 4, wherein the flat distal section is steerable.